Run ID: ERR4818394
Sample name:
Date: 01-04-2023 15:31:59
Number of reads: 253137
Percentage reads mapped: 56.49
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.29 | streptomycin |
panD | 4043869 | p.Val138Ala | missense_variant | 0.75 | pyrazinamide |
embB | 4248488 | p.Ala659Thr | missense_variant | 0.5 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5293 | c.54C>A | synonymous_variant | 0.2 |
gyrB | 6394 | p.Gln385His | missense_variant | 0.33 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.43 |
gyrA | 6952 | c.-350C>G | upstream_gene_variant | 0.43 |
gyrA | 6967 | c.-335T>C | upstream_gene_variant | 0.43 |
gyrA | 6973 | c.-329G>C | upstream_gene_variant | 0.5 |
gyrA | 6982 | c.-320A>C | upstream_gene_variant | 0.62 |
gyrA | 7006 | c.-296T>C | upstream_gene_variant | 0.71 |
gyrA | 7007 | c.-295C>T | upstream_gene_variant | 0.71 |
gyrA | 7010 | c.-292C>T | upstream_gene_variant | 0.71 |
gyrA | 7015 | c.-287G>A | upstream_gene_variant | 0.62 |
gyrB | 7023 | p.Leu595Gln | missense_variant | 0.62 |
gyrB | 7028 | p.Ala597Ser | missense_variant | 0.62 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.62 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.67 |
gyrA | 7790 | c.489G>C | synonymous_variant | 0.67 |
gyrA | 7793 | c.492G>C | synonymous_variant | 0.67 |
gyrA | 7796 | c.495G>C | synonymous_variant | 0.5 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.5 |
gyrA | 7814 | c.513C>G | synonymous_variant | 0.5 |
gyrA | 7823 | c.522G>C | synonymous_variant | 0.5 |
gyrA | 8090 | c.789C>A | synonymous_variant | 0.5 |
gyrA | 8093 | c.792C>T | synonymous_variant | 0.5 |
gyrA | 8096 | c.795T>A | synonymous_variant | 0.5 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.6 |
gyrA | 8121 | c.820T>C | synonymous_variant | 1.0 |
gyrA | 8129 | c.828T>C | synonymous_variant | 1.0 |
gyrA | 8135 | c.834C>G | synonymous_variant | 1.0 |
gyrA | 8156 | c.855T>C | synonymous_variant | 1.0 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.67 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.67 |
gyrA | 8372 | c.1071G>C | synonymous_variant | 0.5 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.6 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.6 |
gyrA | 8387 | c.1086C>T | synonymous_variant | 0.6 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.75 |
gyrA | 8399 | c.1098T>G | synonymous_variant | 0.75 |
gyrA | 8401 | p.Asp367Ala | missense_variant | 0.6 |
gyrA | 8405 | c.1104C>T | synonymous_variant | 0.6 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.75 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.67 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.67 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.33 |
gyrA | 8807 | c.1506C>T | synonymous_variant | 0.5 |
gyrA | 8810 | c.1509A>G | synonymous_variant | 0.5 |
gyrA | 8816 | c.1515C>G | synonymous_variant | 0.57 |
gyrA | 8818 | p.Ser506Asn | missense_variant | 0.57 |
gyrA | 8828 | c.1527T>C | synonymous_variant | 0.67 |
gyrA | 8837 | c.1536C>T | synonymous_variant | 0.67 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.4 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.4 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.38 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.38 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.38 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.43 |
fgd1 | 490797 | c.15G>A | synonymous_variant | 0.29 |
fgd1 | 490800 | c.18A>C | synonymous_variant | 0.29 |
fgd1 | 490803 | c.21T>A | synonymous_variant | 0.29 |
fgd1 | 490812 | c.30A>G | synonymous_variant | 0.29 |
fgd1 | 490815 | c.33G>C | synonymous_variant | 0.29 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.29 |
fgd1 | 490848 | c.66A>G | synonymous_variant | 0.25 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.25 |
fgd1 | 490868 | p.Ala29Gly | missense_variant | 0.29 |
fgd1 | 491313 | c.531C>G | synonymous_variant | 0.75 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.75 |
fgd1 | 491325 | c.543G>C | synonymous_variant | 0.75 |
fgd1 | 491337 | c.555C>G | synonymous_variant | 1.0 |
fgd1 | 491340 | c.558C>G | synonymous_variant | 1.0 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 1.0 |
fgd1 | 491364 | c.582T>C | synonymous_variant | 0.67 |
fgd1 | 491367 | c.585G>C | synonymous_variant | 0.67 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.29 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.33 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.33 |
fgd1 | 491553 | c.771G>A | synonymous_variant | 0.29 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.25 |
fgd1 | 491610 | c.828A>G | synonymous_variant | 0.45 |
fgd1 | 491616 | c.834A>G | synonymous_variant | 0.45 |
fgd1 | 491620 | p.Ile280Val | missense_variant | 0.45 |
fgd1 | 491643 | c.861G>A | synonymous_variant | 0.43 |
fgd1 | 491646 | c.864G>C | synonymous_variant | 0.43 |
fgd1 | 491649 | c.867C>T | synonymous_variant | 0.43 |
fgd1 | 491658 | c.876A>G | synonymous_variant | 0.5 |
fgd1 | 491661 | c.879C>G | synonymous_variant | 0.5 |
fgd1 | 491673 | c.891A>C | synonymous_variant | 0.5 |
fgd1 | 491676 | c.894T>C | synonymous_variant | 0.6 |
fgd1 | 491679 | c.897A>G | synonymous_variant | 0.6 |
mshA | 575156 | c.-192G>C | upstream_gene_variant | 0.18 |
mshA | 575623 | c.276C>G | synonymous_variant | 0.33 |
mshA | 575629 | c.282A>G | synonymous_variant | 0.29 |
mshA | 575632 | c.285G>C | synonymous_variant | 0.29 |
mshA | 575635 | c.288A>C | synonymous_variant | 0.29 |
mshA | 575638 | c.291T>C | synonymous_variant | 0.24 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.24 |
mshA | 575647 | c.300G>C | synonymous_variant | 0.24 |
mshA | 575649 | p.Val101Ala | missense_variant | 0.24 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.33 |
mshA | 575662 | c.315C>G | synonymous_variant | 0.33 |
mshA | 575674 | c.327G>C | synonymous_variant | 0.38 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.25 |
mshA | 575701 | c.354G>A | synonymous_variant | 0.3 |
mshA | 575704 | c.357T>G | synonymous_variant | 0.2 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.2 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.29 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.33 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.33 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.33 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.25 |
mshA | 575864 | c.517T>C | synonymous_variant | 0.27 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.25 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.25 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.25 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.31 |
mshA | 575908 | c.561A>G | synonymous_variant | 0.27 |
mshA | 575917 | p.Asp190Glu | missense_variant | 0.25 |
mshA | 575920 | c.573C>G | synonymous_variant | 0.2 |
mshA | 575924 | p.Gly193Ser | missense_variant | 0.19 |
ccsA | 619916 | p.Gly9Glu | missense_variant | 0.4 |
ccsA | 619923 | c.33C>G | synonymous_variant | 0.33 |
ccsA | 619947 | c.57C>G | synonymous_variant | 0.29 |
ccsA | 619956 | c.66G>C | synonymous_variant | 0.29 |
ccsA | 619959 | c.69G>C | synonymous_variant | 0.25 |
ccsA | 619968 | c.78G>C | synonymous_variant | 0.2 |
ccsA | 619969 | p.Val27Ile | missense_variant | 0.2 |
ccsA | 620710 | p.Val274Ile | missense_variant | 0.33 |
ccsA | 620718 | c.828G>C | synonymous_variant | 0.33 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.33 |
ccsA | 620733 | c.843G>C | synonymous_variant | 0.29 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.29 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.29 |
ccsA | 620742 | c.852G>C | synonymous_variant | 0.29 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.29 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.29 |
ccsA | 620763 | c.873G>A | synonymous_variant | 0.25 |
ccsA | 620769 | c.879C>G | synonymous_variant | 0.25 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.25 |
ccsA | 620784 | c.894C>G | synonymous_variant | 0.25 |
rpoB | 759629 | c.-178T>C | upstream_gene_variant | 0.6 |
rpoB | 759635 | c.-172C>T | upstream_gene_variant | 0.6 |
rpoB | 760040 | c.234T>C | synonymous_variant | 0.6 |
rpoB | 760046 | c.240G>C | synonymous_variant | 0.43 |
rpoB | 760060 | p.Tyr85Leu | missense_variant | 0.33 |
rpoB | 760067 | c.261G>C | synonymous_variant | 0.33 |
rpoB | 760070 | c.264T>G | synonymous_variant | 0.33 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.38 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.5 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.38 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.38 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.38 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.38 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.22 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.33 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.57 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.5 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.43 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.36 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.44 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.3 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.18 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.25 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.25 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.18 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.18 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.17 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.25 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.25 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.25 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.67 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.67 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.6 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.6 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.5 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.6 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.55 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.31 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.31 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.31 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.33 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.36 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.33 |
rpoB | 760718 | c.912C>T | synonymous_variant | 0.22 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.22 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.22 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.5 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.6 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.6 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.67 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.5 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.4 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.4 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.4 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.6 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.6 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.5 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.43 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.5 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.43 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.43 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.38 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.29 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.29 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.67 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.5 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.5 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.4 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.5 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.5 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.5 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.5 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.5 |
rpoC | 762947 | c.-423C>A | upstream_gene_variant | 0.4 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.5 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.5 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.33 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.5 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.5 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.5 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.43 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.36 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.33 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.25 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.25 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.33 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.4 |
rpoC | 763202 | c.-168A>G | upstream_gene_variant | 0.33 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.33 |
rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 0.33 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.33 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.33 |
rpoC | 763227 | c.-143C>T | upstream_gene_variant | 0.33 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.25 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.33 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.29 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.29 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.22 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.29 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.25 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.22 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.2 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.25 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.25 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.43 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.57 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.67 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.57 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.57 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.5 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.6 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.5 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.5 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.43 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.4 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.5 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.5 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.25 |
rpoC | 764195 | p.Ser276Ile | missense_variant | 0.25 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.22 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.25 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.22 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.33 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.25 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.23 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.44 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.33 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.33 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.4 |
rpoC | 764872 | c.1503A>C | synonymous_variant | 0.25 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.29 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.5 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.5 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.5 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.4 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.4 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.4 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.4 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.4 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.4 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.4 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.67 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.75 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.8 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.86 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.5 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.4 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.4 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.4 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.4 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.22 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.88 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.78 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.75 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.7 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.5 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.33 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.22 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.3 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.33 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.27 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.31 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.5 |
rpoC | 766141 | c.2772C>T | synonymous_variant | 0.4 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.4 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.4 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.4 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.4 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.67 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.57 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.57 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.57 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.8 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.83 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.6 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.6 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.6 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.75 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.75 |
rpoC | 766531 | c.3162G>C | synonymous_variant | 0.75 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.67 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.75 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.75 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.75 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.75 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.62 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.5 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.44 |
rpoC | 766673 | p.Gly1102Asn | missense_variant | 0.29 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.44 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.33 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.5 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.46 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.55 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.5 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.57 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.57 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.67 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.67 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.5 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.5 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.4 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.29 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.29 |
rpsL | 781571 | c.12C>T | synonymous_variant | 0.43 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.33 |
rpsL | 781605 | p.Ile16Val | missense_variant | 0.3 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.3 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.33 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.33 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.75 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.75 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.71 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.71 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.75 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.78 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.78 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.75 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.75 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.75 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.78 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.8 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.6 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.6 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.5 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.5 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.5 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.5 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.5 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.4 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.5 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.38 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.33 |
rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.4 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.5 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.44 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.5 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.67 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.57 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.5 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.5 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.36 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.33 |
rplC | 800794 | c.-15A>G | upstream_gene_variant | 0.18 |
rplC | 800796 | c.-13A>G | upstream_gene_variant | 0.18 |
rplC | 800798 | c.-10_-9delGG | upstream_gene_variant | 0.18 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.27 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.27 |
rplC | 800967 | c.159C>G | synonymous_variant | 0.5 |
rplC | 800970 | c.162T>C | synonymous_variant | 0.5 |
rplC | 800982 | c.174C>T | synonymous_variant | 0.5 |
rplC | 800985 | c.177A>G | synonymous_variant | 0.5 |
rplC | 801004 | p.Leu66Val | missense_variant | 0.33 |
rplC | 801009 | c.201A>C | synonymous_variant | 0.33 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.38 |
fbiC | 1303641 | c.711C>T | synonymous_variant | 0.3 |
fbiC | 1303650 | c.720G>C | synonymous_variant | 0.3 |
fbiC | 1303654 | c.724C>T | synonymous_variant | 0.33 |
fbiC | 1303659 | c.729T>C | synonymous_variant | 0.3 |
fbiC | 1303661 | p.Val244Ala | missense_variant | 0.3 |
fbiC | 1303663 | c.733C>T | synonymous_variant | 0.3 |
fbiC | 1303671 | c.741C>T | synonymous_variant | 0.38 |
fbiC | 1303674 | c.744C>G | synonymous_variant | 0.38 |
fbiC | 1303681 | c.751T>C | synonymous_variant | 0.38 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.38 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.38 |
fbiC | 1303704 | c.774T>C | synonymous_variant | 0.38 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.38 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.5 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.4 |
fbiC | 1303842 | c.912C>G | synonymous_variant | 0.4 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.33 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.33 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.33 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.33 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.25 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.25 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.25 |
fbiC | 1304049 | c.1119T>C | synonymous_variant | 0.22 |
fbiC | 1304050 | c.1120T>C | synonymous_variant | 0.22 |
fbiC | 1304058 | c.1128G>A | synonymous_variant | 0.22 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.22 |
fbiC | 1304064 | c.1134G>C | synonymous_variant | 0.22 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.3 |
fbiC | 1304085 | c.1155C>G | synonymous_variant | 0.3 |
fbiC | 1304091 | p.Asp387Glu | missense_variant | 0.3 |
fbiC | 1304092 | p.Met388Leu | missense_variant | 0.33 |
fbiC | 1304097 | c.1167G>C | synonymous_variant | 0.33 |
fbiC | 1304127 | c.1197A>G | synonymous_variant | 0.56 |
fbiC | 1304132 | p.Ala401Gly | missense_variant | 0.5 |
fbiC | 1304142 | c.1212G>C | synonymous_variant | 0.57 |
fbiC | 1304161 | p.Arg411Ser | missense_variant | 0.43 |
fbiC | 1304169 | c.1239T>C | synonymous_variant | 0.38 |
fbiC | 1304174 | p.Val415Ala | missense_variant | 0.33 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.25 |
fbiC | 1304187 | c.1257T>C | synonymous_variant | 0.25 |
fbiC | 1304208 | c.1278C>T | synonymous_variant | 0.15 |
fbiC | 1304309 | p.Thr460Asn | missense_variant | 0.17 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.33 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.5 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.4 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.4 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.33 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.33 |
fbiC | 1304661 | c.1731C>T | synonymous_variant | 0.33 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.4 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.5 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.8 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.8 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.88 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.88 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.88 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.78 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.88 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.83 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.86 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.86 |
fbiC | 1304853 | c.1923C>T | synonymous_variant | 1.0 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 1.0 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.5 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.5 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.4 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.5 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.5 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.5 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.5 |
fbiC | 1304983 | c.2053C>T | synonymous_variant | 0.67 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.5 |
fbiC | 1304995 | p.Leu689Met | missense_variant | 0.5 |
fbiC | 1305297 | c.2367G>C | synonymous_variant | 0.22 |
fbiC | 1305300 | c.2370A>G | synonymous_variant | 0.22 |
fbiC | 1305303 | c.2373T>C | synonymous_variant | 0.22 |
fbiC | 1305306 | c.2376A>T | synonymous_variant | 0.2 |
fbiC | 1305309 | c.2379G>C | synonymous_variant | 0.2 |
fbiC | 1305310 | p.Arg794Glu | missense_variant | 0.22 |
fbiC | 1305318 | c.2388C>G | synonymous_variant | 0.22 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.2 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.22 |
atpE | 1461170 | c.126A>G | synonymous_variant | 0.33 |
atpE | 1461172 | p.Pro43His | missense_variant | 0.33 |
atpE | 1461185 | c.141G>T | synonymous_variant | 0.33 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.4 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.4 |
atpE | 1461233 | c.189A>C | synonymous_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472954 | n.1110delC | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472986 | n.1141_1142insA | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472989 | n.1145delA | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673890 | p.Ala151Ser | missense_variant | 0.3 |
inhA | 1673901 | c.-301A>G | upstream_gene_variant | 0.33 |
fabG1 | 1673905 | p.Ser156Ala | missense_variant | 0.33 |
inhA | 1673916 | c.-286A>C | upstream_gene_variant | 0.45 |
fabG1 | 1673917 | p.Val160Leu | missense_variant | 0.45 |
inhA | 1673922 | c.-280T>C | upstream_gene_variant | 0.45 |
fabG1 | 1673941 | p.Ala168Ser | missense_variant | 0.56 |
inhA | 1673955 | c.-247G>C | upstream_gene_variant | 0.62 |
inhA | 1673961 | c.-241A>C | upstream_gene_variant | 0.62 |
inhA | 1673985 | c.-217C>G | upstream_gene_variant | 0.5 |
fabG1 | 1674006 | p.Asp189Glu | missense_variant | 0.5 |
inhA | 1674504 | c.303C>G | synonymous_variant | 0.5 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.5 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.4 |
inhA | 1674888 | c.687C>G | synonymous_variant | 0.4 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.5 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.5 |
inhA | 1674909 | c.708G>A | synonymous_variant | 0.5 |
inhA | 1674933 | c.732G>C | synonymous_variant | 0.5 |
inhA | 1674942 | c.741T>G | synonymous_variant | 0.5 |
inhA | 1674960 | c.759C>G | synonymous_variant | 0.5 |
inhA | 1674966 | c.765T>G | synonymous_variant | 0.5 |
inhA | 1674967 | p.Asp256Thr | missense_variant | 0.6 |
rpsA | 1833367 | c.-175G>T | upstream_gene_variant | 0.4 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.2 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.23 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.43 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.43 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.55 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.55 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.55 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.5 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.5 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.5 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.5 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.45 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.44 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.44 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.33 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.4 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.4 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.5 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.5 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.4 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.5 |
rpsA | 1834318 | c.777C>A | synonymous_variant | 0.29 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.33 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.3 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.25 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.38 |
rpsA | 1834510 | c.969C>T | synonymous_variant | 0.29 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.29 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.43 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.5 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.43 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.43 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.56 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.5 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.58 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.62 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.62 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.73 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.62 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.33 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.33 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.33 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.5 |
tlyA | 1918248 | c.309T>C | synonymous_variant | 0.3 |
tlyA | 1918251 | c.312T>G | synonymous_variant | 0.3 |
tlyA | 1918258 | p.His107Glu | missense_variant | 0.3 |
tlyA | 1918271 | p.Ala111Val | missense_variant | 0.43 |
tlyA | 1918275 | c.336T>C | synonymous_variant | 0.5 |
tlyA | 1918278 | c.339C>G | synonymous_variant | 0.5 |
tlyA | 1918310 | p.Asn124Ser | missense_variant | 0.6 |
tlyA | 1918315 | p.Pro126Ala | missense_variant | 0.75 |
tlyA | 1918323 | c.384G>C | synonymous_variant | 0.75 |
tlyA | 1918326 | c.387G>C | synonymous_variant | 0.8 |
tlyA | 1918330 | p.Leu131Val | missense_variant | 0.71 |
tlyA | 1918346 | p.Ala136Val | missense_variant | 0.67 |
tlyA | 1918352 | p.Gly138Asp | missense_variant | 0.57 |
tlyA | 1918356 | c.417C>G | synonymous_variant | 0.57 |
tlyA | 1918359 | c.420A>G | synonymous_variant | 0.57 |
tlyA | 1918362 | c.423G>C | synonymous_variant | 0.57 |
tlyA | 1918377 | c.438T>G | synonymous_variant | 0.5 |
tlyA | 1918379 | p.Arg147Pro | missense_variant | 0.5 |
tlyA | 1918382 | p.Val148Ala | missense_variant | 0.5 |
tlyA | 1918389 | c.450G>C | synonymous_variant | 0.5 |
tlyA | 1918392 | c.453A>C | synonymous_variant | 0.5 |
tlyA | 1918422 | c.483T>C | synonymous_variant | 0.33 |
tlyA | 1918425 | c.486C>A | synonymous_variant | 0.22 |
ndh | 2101756 | c.1287G>C | synonymous_variant | 0.29 |
ndh | 2101765 | c.1278C>G | synonymous_variant | 0.33 |
ndh | 2101768 | c.1275C>A | synonymous_variant | 0.33 |
ndh | 2101771 | c.1272T>G | synonymous_variant | 0.33 |
ndh | 2101774 | c.1269T>C | synonymous_variant | 0.33 |
ndh | 2101777 | c.1266C>G | synonymous_variant | 0.33 |
ndh | 2101783 | c.1260T>A | synonymous_variant | 0.57 |
ndh | 2101804 | c.1239T>G | synonymous_variant | 0.8 |
ndh | 2101808 | p.Thr412Ser | missense_variant | 1.0 |
ndh | 2102623 | c.420C>G | synonymous_variant | 0.29 |
ndh | 2102638 | c.405A>C | synonymous_variant | 0.29 |
ndh | 2102644 | c.399A>G | synonymous_variant | 0.29 |
ndh | 2102671 | c.372T>G | synonymous_variant | 0.4 |
ndh | 2102680 | c.363T>C | synonymous_variant | 0.29 |
ndh | 2102686 | c.357G>C | synonymous_variant | 0.4 |
ndh | 2102695 | c.348C>T | synonymous_variant | 0.4 |
ndh | 2102700 | c.343C>T | synonymous_variant | 0.4 |
ndh | 2102710 | c.333C>T | synonymous_variant | 0.33 |
ndh | 2102845 | c.198A>G | synonymous_variant | 0.4 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.67 |
katG | 2155661 | p.Val151Ile | missense_variant | 0.67 |
katG | 2155677 | c.435C>G | synonymous_variant | 0.67 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.67 |
katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
katG | 2155695 | c.417C>G | synonymous_variant | 1.0 |
katG | 2155704 | c.408C>G | synonymous_variant | 1.0 |
katG | 2155716 | c.396T>G | synonymous_variant | 0.67 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.67 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.6 |
katG | 2155740 | p.Gly124Gln | missense_variant | 0.5 |
katG | 2155743 | c.369G>C | synonymous_variant | 0.5 |
katG | 2155981 | p.Asn44Ser | missense_variant | 0.4 |
pncA | 2289308 | c.-67C>T | upstream_gene_variant | 0.25 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.33 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.33 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.33 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.33 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.4 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.4 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.4 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.67 |
kasA | 2518777 | c.663C>T | synonymous_variant | 1.0 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.6 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.5 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.5 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.5 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.5 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.4 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 0.5 |
ahpC | 2726216 | c.24T>C | synonymous_variant | 0.5 |
ahpC | 2726219 | c.27A>G | synonymous_variant | 0.5 |
ahpC | 2726232 | p.Gln14Glu | missense_variant | 0.67 |
ahpC | 2726243 | c.51T>G | synonymous_variant | 0.67 |
ahpC | 2726244 | c.52_54delCTCinsTTG | synonymous_variant | 0.67 |
ahpC | 2726251 | p.Gly20Ala | missense_variant | 0.67 |
ahpC | 2726255 | c.63T>C | synonymous_variant | 0.67 |
ahpC | 2726258 | c.66C>T | synonymous_variant | 0.67 |
ahpC | 2726303 | c.111T>C | synonymous_variant | 1.0 |
ahpC | 2726311 | p.Ser40Asn | missense_variant | 1.0 |
ahpC | 2726315 | p.Asp41Glu | missense_variant | 1.0 |
ahpC | 2726318 | p.Glu42Asp | missense_variant | 1.0 |
ahpC | 2726322 | p.Pro44Ala | missense_variant | 1.0 |
ahpC | 2726330 | c.138G>A | synonymous_variant | 0.67 |
ahpC | 2726336 | c.144G>C | synonymous_variant | 0.67 |
ahpC | 2726348 | c.156T>C | synonymous_variant | 0.67 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.5 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.6 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.6 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.5 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 0.5 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 0.5 |
ahpC | 2726681 | c.489A>C | synonymous_variant | 0.5 |
ahpC | 2726687 | c.495C>G | synonymous_variant | 0.4 |
ahpC | 2726693 | c.501C>G | synonymous_variant | 0.4 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.4 |
folC | 2746375 | c.1224G>C | synonymous_variant | 0.21 |
folC | 2746390 | c.1209G>C | synonymous_variant | 0.2 |
folC | 2746393 | c.1206C>G | synonymous_variant | 0.2 |
folC | 2746401 | p.Ser400Ala | missense_variant | 0.21 |
folC | 2746402 | c.1197T>C | synonymous_variant | 0.21 |
folC | 2746414 | p.Glu395Gln | missense_variant | 0.21 |
folC | 2746420 | c.1179A>C | synonymous_variant | 0.21 |
folC | 2746426 | c.1173G>C | synonymous_variant | 0.23 |
folC | 2746438 | c.1161G>C | synonymous_variant | 0.25 |
folC | 2746451 | p.Gly383Ala | missense_variant | 0.25 |
folC | 2747015 | c.583dupA | frameshift_variant | 0.22 |
folC | 2747302 | c.297A>C | synonymous_variant | 0.29 |
folC | 2747314 | c.285A>C | synonymous_variant | 0.29 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.29 |
folC | 2747332 | c.267G>T | synonymous_variant | 0.25 |
folC | 2747335 | c.264G>C | synonymous_variant | 0.29 |
folC | 2747343 | p.Val86Ile | missense_variant | 0.33 |
pepQ | 2860407 | c.12C>A | synonymous_variant | 0.67 |
pepQ | 2860420 | c.-2T>C | upstream_gene_variant | 0.5 |
pepQ | 2860421 | c.-3G>C | upstream_gene_variant | 0.5 |
pepQ | 2860422 | c.-4G>A | upstream_gene_variant | 0.5 |
pepQ | 2860444 | c.-26C>A | upstream_gene_variant | 0.25 |
pepQ | 2860445 | c.-27T>A | upstream_gene_variant | 0.22 |
pepQ | 2860446 | c.-28T>A | upstream_gene_variant | 0.22 |
pepQ | 2860447 | c.-29A>C | upstream_gene_variant | 0.22 |
pepQ | 2860449 | c.-31G>C | upstream_gene_variant | 0.22 |
pepQ | 2860456 | c.-38G>C | upstream_gene_variant | 0.22 |
pepQ | 2860475 | c.-57C>T | upstream_gene_variant | 0.2 |
pepQ | 2860480 | c.-62G>A | upstream_gene_variant | 0.2 |
pepQ | 2860483 | c.-65A>T | upstream_gene_variant | 0.2 |
pepQ | 2860490 | c.-72G>C | upstream_gene_variant | 0.2 |
ribD | 2987026 | p.Ala63Gly | missense_variant | 0.33 |
ribD | 2987033 | c.195C>G | synonymous_variant | 0.33 |
ribD | 2987042 | c.204A>G | synonymous_variant | 0.3 |
ribD | 2987046 | p.Val70Ile | missense_variant | 0.3 |
ribD | 2987058 | c.220T>C | synonymous_variant | 0.27 |
ribD | 2987066 | c.228A>G | synonymous_variant | 0.27 |
ribD | 2987069 | c.231T>C | synonymous_variant | 0.27 |
ribD | 2987092 | p.Val85Ala | missense_variant | 0.27 |
ribD | 2987105 | c.267C>G | synonymous_variant | 0.18 |
ribD | 2987108 | c.270T>C | synonymous_variant | 0.2 |
Rv2752c | 3064962 | c.1230C>G | synonymous_variant | 0.29 |
Rv2752c | 3064973 | p.Ala407Ser | missense_variant | 0.33 |
Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 0.33 |
Rv2752c | 3065397 | c.795G>C | synonymous_variant | 0.33 |
Rv2752c | 3065400 | c.792A>C | synonymous_variant | 0.33 |
Rv2752c | 3065415 | c.777G>A | synonymous_variant | 0.29 |
Rv2752c | 3065418 | c.774A>G | synonymous_variant | 0.29 |
Rv2752c | 3065442 | c.750T>C | synonymous_variant | 0.22 |
Rv2752c | 3065451 | c.741G>A | synonymous_variant | 0.22 |
Rv2752c | 3065457 | c.735A>C | synonymous_variant | 0.22 |
Rv2752c | 3065463 | c.729T>C | synonymous_variant | 0.22 |
Rv2752c | 3065925 | p.Ala89Gly | missense_variant | 0.67 |
Rv2752c | 3065928 | c.264G>C | synonymous_variant | 1.0 |
Rv2752c | 3065946 | p.Gly82Ala | missense_variant | 0.75 |
Rv2752c | 3065955 | c.235_237delTTGinsCTC | synonymous_variant | 0.6 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.6 |
Rv2752c | 3065988 | c.204A>G | synonymous_variant | 0.6 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.5 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.5 |
Rv2752c | 3066003 | c.189C>T | synonymous_variant | 0.4 |
Rv2752c | 3066009 | c.183G>C | synonymous_variant | 0.4 |
Rv2752c | 3066018 | c.174T>C | synonymous_variant | 0.57 |
Rv2752c | 3066024 | c.168T>G | synonymous_variant | 0.5 |
Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.43 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.43 |
Rv2752c | 3066045 | c.147T>C | synonymous_variant | 0.5 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.5 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.62 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.56 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.56 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.33 |
Rv2752c | 3066330 | c.-139G>C | upstream_gene_variant | 0.27 |
Rv2752c | 3066335 | c.-144T>C | upstream_gene_variant | 0.31 |
Rv2752c | 3066339 | c.-148G>C | upstream_gene_variant | 0.36 |
Rv2752c | 3066351 | c.-160G>C | upstream_gene_variant | 0.31 |
Rv2752c | 3066357 | c.-166G>C | upstream_gene_variant | 0.31 |
Rv2752c | 3066360 | c.-169T>C | upstream_gene_variant | 0.31 |
Rv2752c | 3066369 | c.-180_-178delAGCinsGCG | upstream_gene_variant | 0.36 |
Rv2752c | 3066380 | c.-189A>G | upstream_gene_variant | 0.36 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.22 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.3 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.36 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.29 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.33 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.4 |
thyX | 3067462 | c.484C>T | synonymous_variant | 0.4 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.33 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.43 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.43 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.43 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.5 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.67 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.7 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.7 |
thyX | 3067556 | p.His130Gln | missense_variant | 0.7 |
thyX | 3067559 | c.387C>G | synonymous_variant | 0.64 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.7 |
thyX | 3067570 | p.Ala126Pro | missense_variant | 0.67 |
thyX | 3067577 | c.369G>A | synonymous_variant | 0.62 |
thyX | 3067601 | p.Arg115His | missense_variant | 0.78 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.67 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.71 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.71 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.67 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.71 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.71 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.5 |
thyX | 3067691 | p.Ile85Met | missense_variant | 0.29 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.22 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.22 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.22 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.33 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.33 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.36 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.4 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.38 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.38 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.38 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.4 |
thyA | 3073791 | c.681T>C | synonymous_variant | 0.25 |
thyA | 3073794 | c.678A>C | synonymous_variant | 0.25 |
thyA | 3073812 | c.660C>G | synonymous_variant | 0.29 |
thyA | 3073815 | c.657G>A | synonymous_variant | 0.29 |
thyA | 3073824 | c.648A>G | synonymous_variant | 0.25 |
thyA | 3073827 | c.645A>G | synonymous_variant | 0.25 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.33 |
thyA | 3073860 | c.612C>G | synonymous_variant | 0.33 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.29 |
thyA | 3073898 | p.Ala192Ser | missense_variant | 0.22 |
thyA | 3073917 | c.555C>G | synonymous_variant | 0.17 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.18 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.18 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.25 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.27 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.27 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.27 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.3 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.33 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.29 |
thyA | 3074249 | p.His75Asp | missense_variant | 0.67 |
ald | 3087272 | c.453A>C | synonymous_variant | 0.5 |
ald | 3087278 | p.Gln153His | missense_variant | 0.5 |
ald | 3087281 | c.462G>C | synonymous_variant | 0.5 |
ald | 3087284 | c.465C>G | synonymous_variant | 0.5 |
ald | 3087290 | c.471T>C | synonymous_variant | 0.5 |
ald | 3087305 | c.486G>C | synonymous_variant | 0.75 |
ald | 3087311 | c.492C>G | synonymous_variant | 0.75 |
ald | 3087318 | p.Glu167Lys | missense_variant | 0.6 |
ald | 3087344 | c.525C>G | synonymous_variant | 0.6 |
ald | 3087347 | c.528C>G | synonymous_variant | 0.6 |
ald | 3087350 | c.531C>T | synonymous_variant | 0.6 |
ald | 3087356 | c.537C>G | synonymous_variant | 0.6 |
fbiD | 3339546 | c.429G>C | synonymous_variant | 0.18 |
Rv3083 | 3449938 | p.Asp479Tyr | missense_variant | 0.2 |
fprA | 3474444 | c.438G>A | synonymous_variant | 0.4 |
fbiB | 3642581 | c.1047A>C | synonymous_variant | 0.18 |
fbiB | 3642587 | p.Met351Ile | missense_variant | 0.2 |
fbiB | 3642593 | c.1059G>T | synonymous_variant | 0.22 |
fbiB | 3642602 | c.1068A>C | synonymous_variant | 0.2 |
fbiB | 3642605 | c.1071A>C | synonymous_variant | 0.2 |
fbiB | 3642609 | c.1075_1076delAGinsTC | synonymous_variant | 0.25 |
fbiB | 3642614 | c.1080C>T | synonymous_variant | 0.25 |
fbiB | 3642617 | c.1083C>G | synonymous_variant | 0.25 |
fbiB | 3642620 | c.1086T>C | synonymous_variant | 0.25 |
fbiB | 3642656 | c.1122G>C | synonymous_variant | 0.5 |
fbiB | 3642659 | c.1125C>G | synonymous_variant | 0.5 |
fbiB | 3642668 | c.1134A>G | synonymous_variant | 0.57 |
fbiB | 3642677 | c.1143A>G | synonymous_variant | 0.43 |
fbiB | 3642680 | c.1146A>G | synonymous_variant | 0.43 |
fbiB | 3642684 | c.1150T>C | synonymous_variant | 0.5 |
fbiB | 3642701 | c.1167C>G | synonymous_variant | 0.5 |
fbiB | 3642719 | c.1185T>C | synonymous_variant | 0.56 |
fbiB | 3642731 | c.1197C>G | synonymous_variant | 0.5 |
fbiB | 3642743 | c.1209T>C | synonymous_variant | 0.33 |
fbiB | 3642749 | c.1215T>C | synonymous_variant | 0.4 |
fbiB | 3642758 | c.1224C>G | synonymous_variant | 0.33 |
fbiB | 3642763 | p.Asp410Ala | missense_variant | 0.29 |
fbiB | 3642770 | c.1236G>C | synonymous_variant | 0.29 |
fbiB | 3642779 | c.1245A>C | synonymous_variant | 0.33 |
fbiB | 3642781 | p.Val416Ala | missense_variant | 0.33 |
alr | 3841241 | c.180G>A | synonymous_variant | 0.67 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.2 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.4 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.45 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.3 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.29 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.29 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.29 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.29 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.4 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.4 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.33 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.33 |
rpoA | 3877785 | c.723C>G | synonymous_variant | 0.5 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.5 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.6 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.6 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.5 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.5 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.6 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.6 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.6 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.6 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.6 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.6 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.8 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.8 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.67 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.4 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.4 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.4 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.33 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.33 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.33 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.33 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.43 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.43 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.38 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.38 |
rpoA | 3878226 | c.282C>G | synonymous_variant | 0.29 |
rpoA | 3878232 | c.276G>C | synonymous_variant | 0.33 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.29 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.29 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.29 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.33 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.4 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.4 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.5 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.5 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.5 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.5 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.67 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.5 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.5 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.4 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.4 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.33 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.29 |
ddn | 3986645 | c.-199G>A | upstream_gene_variant | 0.38 |
ddn | 3986646 | c.-198_-196delCTCinsTTG | upstream_gene_variant | 0.43 |
ddn | 3986665 | c.-179G>C | upstream_gene_variant | 0.33 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.33 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.33 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.36 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.4 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.43 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.33 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.33 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.36 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.55 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.5 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.4 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.2 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.2 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.18 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.17 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.17 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.18 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.18 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.2 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.33 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.33 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.4 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.53 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.62 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.67 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.64 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.64 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.7 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.7 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.8 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.8 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.57 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.5 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.5 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.5 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.5 |
clpC1 | 4039217 | c.1488G>C | synonymous_variant | 0.33 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.38 |
clpC1 | 4039241 | c.1464G>C | synonymous_variant | 0.4 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.5 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.55 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.62 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.62 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.62 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.62 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.83 |
clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.83 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.67 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.5 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.56 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.5 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.38 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.44 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.38 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.33 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.3 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.25 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.36 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.42 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.38 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.38 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.38 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.46 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.46 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.56 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.45 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.45 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.5 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.5 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.45 |
clpC1 | 4039576 | p.Ala377Pro | missense_variant | 0.45 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.45 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.46 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.2 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.25 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.27 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.27 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.27 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.36 |
clpC1 | 4039700 | c.1005C>T | synonymous_variant | 0.25 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.23 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.27 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.2 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.2 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.2 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.2 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.2 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.2 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.18 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.25 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.27 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.44 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.55 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.5 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.4 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.62 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.45 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.45 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.5 |
clpC1 | 4039946 | p.Gly253Val | missense_variant | 0.5 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.5 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.57 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.57 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.57 |
clpC1 | 4039994 | c.711G>A | synonymous_variant | 0.4 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.33 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.33 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.5 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.5 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.4 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.4 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.33 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.33 |
panD | 4043865 | p.Gly139Arg | missense_variant | 0.75 |
panD | 4043872 | p.Gly137Val | missense_variant | 0.75 |
panD | 4043876 | p.Leu136Ile | missense_variant | 0.75 |
panD | 4043883 | c.399C>T | synonymous_variant | 0.6 |
panD | 4043886 | c.396A>G | synonymous_variant | 0.6 |
panD | 4043896 | p.Gly129Ala | missense_variant | 0.75 |
panD | 4043903 | p.Asn127Asp | missense_variant | 0.75 |
panD | 4043913 | c.369T>C | synonymous_variant | 0.75 |
panD | 4043916 | c.366A>G | synonymous_variant | 0.75 |
embC | 4241038 | c.1176G>C | synonymous_variant | 0.25 |
embC | 4241047 | c.1185C>G | synonymous_variant | 0.29 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.29 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.25 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.56 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.56 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.6 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.56 |
embC | 4241146 | c.1284C>G | synonymous_variant | 0.45 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.5 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.5 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.5 |
embC | 4241170 | c.1308G>C | synonymous_variant | 0.36 |
embC | 4241173 | c.1311C>T | synonymous_variant | 0.36 |
embC | 4241293 | c.1431G>T | synonymous_variant | 0.29 |
embC | 4241394 | p.Lys511Ser | missense_variant | 0.5 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.5 |
embC | 4241479 | c.1617C>G | synonymous_variant | 0.5 |
embC | 4241480 | c.1618T>C | synonymous_variant | 0.5 |
embC | 4241488 | c.1626G>C | synonymous_variant | 0.4 |
embC | 4241496 | p.Ala545Gly | missense_variant | 0.33 |
embC | 4241500 | c.1638A>C | synonymous_variant | 0.33 |
embC | 4241501 | p.Ser547Thr | missense_variant | 0.33 |
embC | 4241506 | c.1644G>C | synonymous_variant | 0.33 |
embA | 4242715 | c.-518T>C | upstream_gene_variant | 0.2 |
embA | 4242742 | c.-491C>G | upstream_gene_variant | 0.38 |
embA | 4242748 | c.-485A>G | upstream_gene_variant | 0.43 |
embA | 4242754 | c.-479G>C | upstream_gene_variant | 0.43 |
embC | 4242764 | p.Val968Leu | missense_variant | 0.5 |
embA | 4242772 | c.-461G>C | upstream_gene_variant | 0.5 |
embC | 4242779 | p.Asn973Asp | missense_variant | 0.57 |
embC | 4242791 | p.Ala977Ser | missense_variant | 0.83 |
embA | 4242796 | c.-437G>C | upstream_gene_variant | 0.83 |
embA | 4242799 | c.-434T>C | upstream_gene_variant | 0.83 |
embA | 4242820 | c.-413G>C | upstream_gene_variant | 0.56 |
embA | 4242823 | c.-410G>C | upstream_gene_variant | 0.44 |
embA | 4242832 | c.-401A>C | upstream_gene_variant | 0.44 |
embA | 4242838 | c.-395C>G | upstream_gene_variant | 0.44 |
embA | 4242841 | c.-392C>T | upstream_gene_variant | 0.44 |
embA | 4242844 | c.-389A>G | upstream_gene_variant | 0.44 |
embA | 4242847 | c.-386C>A | upstream_gene_variant | 0.44 |
embA | 4242859 | c.-374C>T | upstream_gene_variant | 0.4 |
embA | 4242862 | c.-371A>G | upstream_gene_variant | 0.4 |
embC | 4242863 | p.Tyr1001Asn | missense_variant | 0.4 |
embA | 4242883 | c.-350C>G | upstream_gene_variant | 0.2 |
embA | 4242892 | c.-341G>C | upstream_gene_variant | 0.25 |
embA | 4242901 | c.-332G>C | upstream_gene_variant | 0.22 |
embA | 4242919 | c.-314A>G | upstream_gene_variant | 0.25 |
embA | 4242928 | c.-305A>G | upstream_gene_variant | 0.29 |
embA | 4242931 | c.-302G>C | upstream_gene_variant | 0.29 |
embA | 4242940 | c.-293T>C | upstream_gene_variant | 0.29 |
embC | 4242941 | p.His1027Asn | missense_variant | 0.29 |
embA | 4242946 | c.-287T>C | upstream_gene_variant | 0.29 |
embA | 4242952 | c.-281T>C | upstream_gene_variant | 0.29 |
embC | 4242965 | p.Ile1035Val | missense_variant | 0.33 |
embA | 4243291 | c.62delG | frameshift_variant | 0.5 |
embA | 4244306 | c.1074G>C | synonymous_variant | 0.67 |
embA | 4244312 | c.1080T>G | synonymous_variant | 0.67 |
embA | 4244315 | c.1083G>C | synonymous_variant | 0.5 |
embA | 4244324 | c.1092T>G | synonymous_variant | 0.4 |
embA | 4244327 | c.1095T>C | synonymous_variant | 0.4 |
embA | 4244337 | p.Leu369Val | missense_variant | 0.33 |
embA | 4244340 | p.Ser370Ala | missense_variant | 0.33 |
embA | 4244366 | c.1134C>G | synonymous_variant | 0.22 |
embA | 4244372 | c.1140T>G | synonymous_variant | 0.22 |
embA | 4244378 | c.1146G>A | synonymous_variant | 0.22 |
embA | 4244671 | p.Ala480Val | missense_variant | 0.29 |
embA | 4245041 | c.1809C>G | synonymous_variant | 0.22 |
embA | 4245044 | c.1812G>C | synonymous_variant | 0.22 |
embA | 4245053 | c.1821G>C | synonymous_variant | 0.3 |
embA | 4245060 | c.1828T>C | synonymous_variant | 0.36 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.57 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.5 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.44 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.33 |
embB | 4245983 | c.-531A>C | upstream_gene_variant | 0.38 |
embB | 4245989 | c.-525A>G | upstream_gene_variant | 0.44 |
embB | 4245992 | c.-522C>G | upstream_gene_variant | 0.5 |
embB | 4246004 | c.-510T>C | upstream_gene_variant | 0.5 |
embB | 4246010 | c.-504G>T | upstream_gene_variant | 0.5 |
embB | 4246013 | c.-501T>C | upstream_gene_variant | 0.5 |
embB | 4246040 | c.-474C>G | upstream_gene_variant | 0.5 |
embA | 4246041 | p.Asp937Asn | missense_variant | 0.5 |
embB | 4246055 | c.-459T>C | upstream_gene_variant | 0.5 |
embB | 4246064 | c.-450T>C | upstream_gene_variant | 0.56 |
embA | 4246080 | p.Pro950Ser | missense_variant | 0.44 |
embB | 4246250 | c.-264G>C | upstream_gene_variant | 0.33 |
embB | 4246256 | c.-258G>T | upstream_gene_variant | 0.38 |
embB | 4246259 | c.-255G>C | upstream_gene_variant | 0.38 |
embA | 4246264 | p.His1011Arg | missense_variant | 0.43 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.38 |
embA | 4246305 | p.Ser1025Glu | missense_variant | 0.33 |
embA | 4246308 | p.Thr1026Ala | missense_variant | 0.33 |
embB | 4246316 | c.-198T>G | upstream_gene_variant | 0.29 |
embB | 4246319 | c.-195G>C | upstream_gene_variant | 0.38 |
embA | 4246329 | p.Thr1033Ala | missense_variant | 0.4 |
embB | 4246349 | c.-165C>G | upstream_gene_variant | 0.4 |
embA | 4246359 | p.Ala1043Ser | missense_variant | 0.4 |
embB | 4246367 | c.-147C>T | upstream_gene_variant | 0.29 |
embB | 4246373 | c.-141T>C | upstream_gene_variant | 0.25 |
embB | 4246376 | c.-138G>C | upstream_gene_variant | 0.25 |
embB | 4246379 | c.-135C>T | upstream_gene_variant | 0.25 |
embB | 4247046 | c.537delC | frameshift_variant | 0.5 |
embB | 4247746 | c.1233C>T | synonymous_variant | 0.2 |
embB | 4247761 | c.1248T>C | synonymous_variant | 0.33 |
embB | 4247773 | c.1260G>A | synonymous_variant | 0.36 |
embB | 4247776 | c.1263G>T | synonymous_variant | 0.43 |
embB | 4247797 | c.1284C>G | synonymous_variant | 0.57 |
embB | 4247800 | c.1287A>T | synonymous_variant | 0.54 |
embB | 4247803 | c.1290G>C | synonymous_variant | 0.58 |
embB | 4247815 | c.1302C>G | synonymous_variant | 0.58 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.58 |
embB | 4247830 | c.1317A>G | synonymous_variant | 0.75 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.75 |
embB | 4247839 | c.1326G>C | synonymous_variant | 0.75 |
embB | 4247875 | c.1362G>C | synonymous_variant | 0.78 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.86 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.86 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.83 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.83 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.88 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.88 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.78 |
embB | 4247914 | c.1401G>C | synonymous_variant | 0.7 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.7 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.56 |
embB | 4247945 | c.1432T>C | synonymous_variant | 0.56 |
embB | 4247951 | p.Ser480Ala | missense_variant | 0.56 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.56 |
embB | 4247974 | c.1461C>G | synonymous_variant | 0.38 |
embB | 4247983 | c.1470G>T | synonymous_variant | 0.29 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.29 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.29 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.4 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.33 |
embB | 4248139 | c.1626C>G | synonymous_variant | 0.33 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.33 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.33 |
embB | 4248147 | p.Ile545Asn | missense_variant | 0.29 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.5 |
embB | 4248172 | c.1659G>C | synonymous_variant | 0.29 |
embB | 4248199 | c.1686A>G | synonymous_variant | 0.43 |
embB | 4248200 | p.Ile563Val | missense_variant | 0.43 |
embB | 4248205 | c.1692C>G | synonymous_variant | 0.43 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.43 |
embB | 4248220 | c.1707A>C | synonymous_variant | 0.6 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.3 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.3 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.3 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.27 |
embB | 4248373 | c.1860C>G | synonymous_variant | 0.4 |
embB | 4248407 | p.Leu632Val | missense_variant | 0.5 |
embB | 4248410 | p.Phe633Leu | missense_variant | 0.5 |
embB | 4248419 | p.Leu636Met | missense_variant | 0.5 |
embB | 4248430 | c.1917T>C | synonymous_variant | 0.5 |
embB | 4248432 | p.Trp640Phe | missense_variant | 0.5 |
embB | 4248457 | c.1944T>C | synonymous_variant | 0.71 |
embB | 4248472 | c.1959T>C | synonymous_variant | 0.67 |
embB | 4248475 | c.1962G>C | synonymous_variant | 0.5 |
embB | 4248504 | p.Asp664Gly | missense_variant | 0.5 |
embB | 4248508 | c.1995G>A | synonymous_variant | 0.5 |
embB | 4248512 | p.Thr667Ser | missense_variant | 0.5 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.33 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.4 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.4 |
embB | 4249429 | c.2916C>T | synonymous_variant | 0.4 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.4 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.29 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.4 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.4 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.5 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.62 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.5 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.45 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.45 |
embB | 4249529 | p.Ile1006Val | missense_variant | 0.45 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.45 |
embB | 4249537 | c.3024A>G | synonymous_variant | 0.5 |
embB | 4249543 | c.3030G>C | synonymous_variant | 0.56 |
embB | 4249546 | c.3033G>A | synonymous_variant | 0.56 |
embB | 4249558 | c.3045A>C | synonymous_variant | 0.33 |
embB | 4249568 | p.Ser1019Thr | missense_variant | 0.38 |
ethA | 4326698 | p.Arg259Leu | missense_variant | 0.4 |
ethA | 4328463 | c.-990G>C | upstream_gene_variant | 0.29 |
ethA | 4328467 | c.-994G>T | upstream_gene_variant | 0.33 |
ethA | 4328470 | c.-998_-997delAGinsGC | upstream_gene_variant | 0.33 |