Run ID: SRR13861528
Sample name:
Date: 03-04-2023 09:34:07
Number of reads: 645150
Percentage reads mapped: 64.58
Strain: lineage4.9
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.16 | streptomycin |
katG | 2154411 | c.1700delT | frameshift_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6223 | c.984G>C | synonymous_variant | 0.18 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.15 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.16 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.17 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.17 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.17 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.17 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.16 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.16 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.16 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.17 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.15 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.14 |
gyrA | 7949 | c.648G>T | synonymous_variant | 0.93 |
gyrA | 8096 | c.795T>C | synonymous_variant | 0.15 |
gyrA | 8123 | p.Leu274Phe | missense_variant | 0.88 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.17 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.14 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.15 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.17 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.14 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.2 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.2 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.19 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.19 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.2 |
gyrA | 8717 | c.1416C>G | synonymous_variant | 0.2 |
gyrA | 8720 | c.1419G>A | synonymous_variant | 0.2 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.21 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.22 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.21 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.17 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.18 |
gyrA | 8765 | p.Asp488Glu | missense_variant | 0.17 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.17 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.14 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.2 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.18 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.14 |
gyrA | 8816 | c.1515C>T | synonymous_variant | 0.14 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.14 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.14 |
gyrA | 9278 | c.1977G>C | synonymous_variant | 0.14 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.15 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.14 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.14 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.13 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.17 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.16 |
gyrA | 9768 | p.Gly823Cys | missense_variant | 1.0 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.15 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.15 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.15 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.14 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.18 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.18 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.19 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.2 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.17 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.21 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.21 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.22 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.21 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.21 |
fgd1 | 491301 | c.519C>T | synonymous_variant | 0.21 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.17 |
mshA | 575587 | c.240C>A | synonymous_variant | 0.19 |
mshA | 575623 | c.276C>G | synonymous_variant | 0.22 |
mshA | 575629 | c.282A>C | synonymous_variant | 0.24 |
mshA | 575635 | c.288A>C | synonymous_variant | 0.19 |
mshA | 575638 | c.291T>C | synonymous_variant | 0.18 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.17 |
mshA | 575648 | p.Val101Gln | missense_variant | 0.16 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.17 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.18 |
mshA | 575704 | c.357T>C | synonymous_variant | 0.18 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.18 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.18 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.16 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.18 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.22 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.2 |
mshA | 575752 | c.405G>A | synonymous_variant | 0.21 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.14 |
mshA | 575772 | p.Val142Ala | missense_variant | 0.14 |
ccsA | 620703 | c.813G>C | synonymous_variant | 0.17 |
ccsA | 620710 | p.Val274Ile | missense_variant | 0.15 |
ccsA | 620730 | c.840C>T | synonymous_variant | 0.16 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.14 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.15 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.17 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.16 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.16 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.16 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.17 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.19 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.15 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.14 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.15 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.21 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.28 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.28 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.33 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.29 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.29 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.33 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.31 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.31 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.28 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.24 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.25 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.17 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.18 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.18 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.15 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.15 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.3 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.3 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.35 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.32 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.38 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.39 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.41 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.35 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.25 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.3 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.29 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.35 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.32 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.25 |
rpoC | 763734 | p.Pro122Leu | missense_variant | 0.89 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.14 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.14 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.17 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.17 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.18 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.19 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.19 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.21 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.18 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.24 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.27 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.27 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.24 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.28 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.3 |
rpoC | 764195 | p.Ser276Gln | missense_variant | 0.31 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.33 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.33 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.18 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.17 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.17 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.17 |
rpoC | 764282 | c.913_915delTCGinsAGC | synonymous_variant | 0.17 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.22 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.2 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.17 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.17 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.2 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.21 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.17 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.22 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.15 |
rpoC | 764714 | c.1345C>T | synonymous_variant | 0.14 |
rpoC | 764720 | c.1351C>T | synonymous_variant | 0.14 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.19 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.18 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.2 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.18 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.17 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.18 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.21 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.22 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.3 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.3 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.29 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.28 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.3 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.29 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.32 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.21 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.24 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.27 |
rpoC | 765022 | c.1653G>C | synonymous_variant | 0.29 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.25 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.24 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.24 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.25 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.21 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.21 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.21 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.23 |
rpoC | 765085 | c.1716T>G | synonymous_variant | 0.2 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.2 |
rpoC | 765103 | c.1734G>A | synonymous_variant | 0.23 |
rpoC | 765300 | p.Val644Ala | missense_variant | 0.19 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.16 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.16 |
rpoC | 765330 | p.Ser654Asn | missense_variant | 0.16 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.16 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.19 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.15 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.15 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.15 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.17 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.17 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.18 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.21 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.14 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.14 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.14 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.14 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.15 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.17 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.14 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.17 |
rpoC | 766105 | c.2736C>T | synonymous_variant | 0.17 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.14 |
rpoC | 766141 | c.2772C>T | synonymous_variant | 0.13 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.13 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.15 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.15 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.19 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.16 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.25 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.2 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.22 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.22 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.25 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.25 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.2 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.24 |
rpoC | 766531 | c.3162G>T | synonymous_variant | 0.24 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.23 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.2 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.12 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.13 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.14 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.2 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.15 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.19 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.18 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.17 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.15 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.17 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.16 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.17 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.17 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.2 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.24 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.25 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.17 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.17 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.17 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.17 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.21 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.21 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.17 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.17 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.15 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.14 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.18 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.16 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.21 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.22 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.24 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.2 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.18 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.18 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.18 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.15 |
rplC | 801301 | c.493C>A | synonymous_variant | 0.12 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.17 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.17 |
rplC | 801341 | p.Leu178His | missense_variant | 0.18 |
fbiC | 1304517 | c.1587C>T | synonymous_variant | 0.13 |
fbiC | 1304523 | c.1593G>T | synonymous_variant | 0.13 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.15 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.15 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.17 |
fbiC | 1304574 | c.1644C>G | synonymous_variant | 0.2 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.22 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.15 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.17 |
fbiC | 1304670 | c.1740G>T | synonymous_variant | 0.17 |
fbiC | 1304671 | p.Val581Thr | missense_variant | 0.17 |
fbiC | 1304675 | p.Gly582Glu | missense_variant | 0.18 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.2 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.19 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.17 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.17 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.17 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.17 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.17 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.17 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.17 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.17 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.19 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.19 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 0.18 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.23 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.24 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.25 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.16 |
fbiC | 1304832 | c.1902C>G | synonymous_variant | 0.17 |
fbiC | 1304853 | c.1923C>G | synonymous_variant | 0.16 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.16 |
fbiC | 1304878 | p.Arg650Ser | missense_variant | 0.12 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.16 |
fbiC | 1305276 | c.2346G>C | synonymous_variant | 0.13 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.17 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.17 |
atpE | 1461233 | c.189A>G | synonymous_variant | 0.14 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475015 | n.1358C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475271 | n.1614A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475273 | n.1616T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476640 | n.2983C>A | non_coding_transcript_exon_variant | 0.88 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.14 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.14 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.24 |
inhA | 1674564 | c.363C>T | synonymous_variant | 0.25 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.25 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.25 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.26 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.26 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.26 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.26 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.26 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.27 |
inhA | 1674693 | c.492C>G | synonymous_variant | 0.22 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.23 |
inhA | 1674741 | c.540C>G | synonymous_variant | 0.14 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.14 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.16 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.18 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.19 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.19 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.19 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.18 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.18 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.19 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.24 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.26 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.25 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.19 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.19 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.2 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.2 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.2 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.19 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.18 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.17 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.25 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.16 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.15 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.15 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.2 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.16 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.19 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.19 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.21 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.2 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.2 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.23 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.14 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.14 |
tlyA | 1918034 | p.Val32Ala | missense_variant | 1.0 |
ndh | 2102131 | p.Gln304Lys | missense_variant | 0.14 |
ndh | 2102184 | c.859A>C | synonymous_variant | 0.17 |
ndh | 2102203 | c.840T>A | synonymous_variant | 0.14 |
ndh | 2102206 | c.837G>C | synonymous_variant | 0.14 |
ndh | 2102212 | c.831G>C | synonymous_variant | 0.15 |
ndh | 2102218 | c.825C>G | synonymous_variant | 0.15 |
ndh | 2102233 | c.810G>A | synonymous_variant | 0.14 |
ndh | 2102242 | c.801G>A | synonymous_variant | 0.12 |
katG | 2155918 | p.Ala65Val | missense_variant | 1.0 |
PPE35 | 2168767 | p.Ser616Gly | missense_variant | 1.0 |
Rv1979c | 2222377 | p.Val263Gly | missense_variant | 1.0 |
pncA | 2289958 | c.-717T>C | upstream_gene_variant | 0.19 |
pncA | 2289991 | c.-750G>C | upstream_gene_variant | 0.14 |
pncA | 2289994 | c.-753A>G | upstream_gene_variant | 0.14 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.17 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.14 |
kasA | 2517992 | c.-123C>G | upstream_gene_variant | 0.15 |
kasA | 2518025 | c.-90G>C | upstream_gene_variant | 0.14 |
kasA | 2518031 | c.-84G>T | upstream_gene_variant | 0.14 |
kasA | 2518035 | c.-80C>G | upstream_gene_variant | 0.14 |
kasA | 2518621 | c.507G>A | synonymous_variant | 0.13 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.15 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.15 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.15 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.16 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.19 |
kasA | 2518717 | c.603C>T | synonymous_variant | 0.19 |
kasA | 2518723 | p.Glu203Asp | missense_variant | 0.22 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.24 |
kasA | 2518741 | c.627G>C | synonymous_variant | 0.19 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.18 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.23 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.21 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.2 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.22 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.17 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.18 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.15 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.14 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.19 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.14 |
ribD | 2986993 | p.Gly52Val | missense_variant | 1.0 |
Rv2752c | 3064928 | c.1264T>C | synonymous_variant | 0.14 |
Rv2752c | 3064932 | c.1260T>C | synonymous_variant | 0.14 |
Rv2752c | 3064935 | c.1257A>G | synonymous_variant | 0.14 |
Rv2752c | 3064941 | p.Gln417Glu | missense_variant | 0.16 |
Rv2752c | 3064956 | p.Ser412Arg | missense_variant | 0.16 |
Rv2752c | 3064962 | c.1230C>A | synonymous_variant | 0.17 |
Rv2752c | 3064973 | p.Ala407Ser | missense_variant | 0.15 |
Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 0.15 |
Rv2752c | 3064980 | c.1212C>G | synonymous_variant | 0.14 |
Rv2752c | 3065787 | c.405G>C | synonymous_variant | 1.0 |
thyX | 3067244 | c.702C>G | synonymous_variant | 0.18 |
thyX | 3067252 | p.Val232Met | missense_variant | 0.12 |
thyX | 3067277 | c.669C>G | synonymous_variant | 0.16 |
thyX | 3067284 | p.Ala221Asp | missense_variant | 0.14 |
thyX | 3067640 | c.306G>C | synonymous_variant | 0.14 |
thyX | 3067643 | c.303C>T | synonymous_variant | 0.13 |
thyX | 3067682 | c.264G>C | synonymous_variant | 0.15 |
thyX | 3067685 | c.261A>G | synonymous_variant | 0.15 |
thyX | 3067688 | c.258G>C | synonymous_variant | 0.15 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.15 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.15 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.17 |
thyX | 3067724 | c.222G>A | synonymous_variant | 0.14 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.14 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.14 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.14 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.16 |
thyA | 3074339 | p.Leu45Ile | missense_variant | 0.13 |
thyA | 3074361 | c.111T>C | synonymous_variant | 0.14 |
thyA | 3074409 | c.63C>A | synonymous_variant | 0.13 |
Rv3083 | 3448649 | p.Arg49Pro | missense_variant | 1.0 |
Rv3236c | 3613067 | p.Val17Gly | missense_variant | 1.0 |
Rv3236c | 3613315 | c.-199T>G | upstream_gene_variant | 1.0 |
fbiA | 3640435 | c.-108A>C | upstream_gene_variant | 1.0 |
fbiB | 3642581 | c.1047A>C | synonymous_variant | 0.15 |
fbiB | 3642593 | c.1059G>C | synonymous_variant | 0.14 |
fbiB | 3642602 | c.1068A>C | synonymous_variant | 0.19 |
fbiB | 3642605 | c.1071A>G | synonymous_variant | 0.19 |
fbiB | 3642614 | c.1080C>T | synonymous_variant | 0.17 |
fbiB | 3642620 | c.1086T>C | synonymous_variant | 0.16 |
fbiB | 3642656 | c.1122G>C | synonymous_variant | 0.16 |
fbiB | 3642659 | c.1125C>G | synonymous_variant | 0.16 |
fbiB | 3642668 | c.1134A>C | synonymous_variant | 0.16 |
fbiB | 3642677 | c.1143A>G | synonymous_variant | 0.15 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.16 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.14 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.17 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.16 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.15 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.14 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.15 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.23 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.18 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.18 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.17 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.17 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.16 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.18 |
rpoA | 3878364 | c.144A>G | synonymous_variant | 0.2 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.18 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.18 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.19 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.19 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.19 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.19 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.15 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.15 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.17 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.18 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.19 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.21 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.18 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.17 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.2 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.2 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.2 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.22 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.21 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.23 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.23 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.25 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.25 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.28 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.25 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.23 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.21 |
clpC1 | 4039268 | c.1437C>G | synonymous_variant | 0.17 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.23 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.23 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.23 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.24 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.24 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.19 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.19 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.15 |
clpC1 | 4039842 | c.862_863insT | frameshift_variant | 1.0 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.14 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.16 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.15 |
clpC1 | 4039930 | p.Ser259Cys | missense_variant | 0.14 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.14 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.14 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.16 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.16 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.16 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.17 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.17 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.17 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.2 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.2 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.16 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.16 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.14 |
panD | 4044103 | p.Ile60Ser | missense_variant | 0.91 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.15 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.15 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.16 |
embC | 4240706 | p.Val282Thr | missense_variant | 0.16 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.2 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.19 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.19 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.2 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.15 |
embA | 4245031 | p.Arg600Gln | missense_variant | 1.0 |
embB | 4247842 | c.1329T>C | synonymous_variant | 0.14 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.21 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.16 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.16 |
embB | 4247890 | c.1377C>T | synonymous_variant | 0.17 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.17 |
embB | 4247977 | c.1464C>G | synonymous_variant | 0.14 |
embB | 4247986 | c.1473C>G | synonymous_variant | 0.15 |
embB | 4248007 | c.1494C>G | synonymous_variant | 0.17 |
embB | 4248011 | p.Ser500Ala | missense_variant | 0.14 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.15 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.14 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.15 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.15 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.14 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.19 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.16 |
embB | 4249420 | c.2907G>C | synonymous_variant | 0.15 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.15 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.15 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.17 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.15 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.15 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.15 |
embB | 4249456 | c.2943G>C | synonymous_variant | 0.16 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.15 |
embB | 4249483 | c.2970C>G | synonymous_variant | 0.16 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.16 |
aftB | 4267556 | c.1281G>C | synonymous_variant | 0.21 |
aftB | 4267571 | c.1266T>C | synonymous_variant | 0.18 |
aftB | 4267580 | c.1257G>C | synonymous_variant | 0.18 |
aftB | 4267607 | c.1230G>A | synonymous_variant | 0.16 |
aftB | 4268386 | c.451T>C | synonymous_variant | 0.23 |
aftB | 4268389 | c.448C>T | synonymous_variant | 0.23 |
aftB | 4268396 | c.441T>C | synonymous_variant | 0.23 |
aftB | 4268404 | c.433T>C | synonymous_variant | 0.23 |
aftB | 4268405 | p.Val144Ala | missense_variant | 0.23 |
aftB | 4268410 | c.427C>T | synonymous_variant | 0.21 |
aftB | 4268411 | c.426G>T | synonymous_variant | 0.21 |
aftB | 4268417 | c.420G>A | synonymous_variant | 0.23 |
aftB | 4268441 | c.396C>G | synonymous_variant | 0.25 |
aftB | 4268444 | p.Ala131Ser | missense_variant | 0.25 |
aftB | 4268450 | c.387A>G | synonymous_variant | 0.25 |
aftB | 4268455 | p.Val128Leu | missense_variant | 0.25 |
aftB | 4268462 | c.375T>C | synonymous_variant | 0.25 |
aftB | 4268465 | c.372A>C | synonymous_variant | 0.27 |
aftB | 4268480 | c.357G>C | synonymous_variant | 0.27 |
aftB | 4268483 | c.354T>G | synonymous_variant | 0.27 |
aftB | 4268498 | c.339T>C | synonymous_variant | 0.27 |
aftB | 4268504 | c.333G>C | synonymous_variant | 0.27 |
aftB | 4268516 | c.321A>G | synonymous_variant | 0.25 |
gid | 4408218 | c.-16G>T | upstream_gene_variant | 1.0 |