Run ID: ERR9786592
Sample name:
Date: 02-04-2023 12:34:05
Number of reads: 2126929
Percentage reads mapped: 81.05
Strain: lineage4.3.4.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6817 | c.-485G>A | upstream_gene_variant | 0.99 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.13 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.15 |
gyrA | 8731 | p.Gly477Ala | missense_variant | 0.15 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.17 |
gyrA | 8750 | c.1449C>G | synonymous_variant | 0.17 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.17 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.17 |
gyrA | 8765 | p.Asp488Glu | missense_variant | 0.17 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.18 |
gyrA | 8774 | c.1473C>T | synonymous_variant | 0.21 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.19 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.19 |
gyrA | 8799 | p.Ala500Pro | missense_variant | 0.2 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.19 |
gyrA | 8828 | c.1527T>C | synonymous_variant | 0.18 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.18 |
gyrA | 8840 | c.1539C>G | synonymous_variant | 0.18 |
gyrA | 8843 | c.1542G>A | synonymous_variant | 0.18 |
gyrA | 8852 | c.1551T>G | synonymous_variant | 0.17 |
gyrA | 8858 | c.1557T>G | synonymous_variant | 0.19 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.19 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.17 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.19 |
gyrA | 8909 | c.1608C>T | synonymous_variant | 0.19 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.19 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.17 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.15 |
gyrA | 8952 | p.Gln551Ala | missense_variant | 0.14 |
gyrA | 8967 | p.Ala556Asn | missense_variant | 0.14 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.14 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.14 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.14 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491133 | c.351A>C | synonymous_variant | 0.14 |
fgd1 | 491138 | p.Glu119Ala | missense_variant | 0.14 |
fgd1 | 491142 | c.360C>G | synonymous_variant | 0.14 |
fgd1 | 491144 | p.Ala121Asp | missense_variant | 0.14 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.13 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.13 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.14 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.16 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.15 |
rpoB | 760316 | c.510C>G | synonymous_variant | 0.16 |
rpoB | 760325 | c.519G>C | synonymous_variant | 0.16 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.16 |
rpoB | 760334 | c.528G>T | synonymous_variant | 0.16 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.17 |
rpoB | 760357 | p.Thr184Ser | missense_variant | 0.17 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.17 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.18 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.23 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.23 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.2 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.17 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.15 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.18 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.17 |
rpoB | 760478 | c.672C>T | synonymous_variant | 0.17 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.17 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.17 |
rpoB | 760514 | c.708C>T | synonymous_variant | 0.18 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.16 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.16 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.16 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.19 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.16 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.16 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 0.16 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.17 |
rpoB | 760585 | p.Asn260Ser | missense_variant | 0.17 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.17 |
rpoB | 760595 | c.789C>T | synonymous_variant | 0.17 |
rpoB | 760596 | p.Thr264Pro | missense_variant | 0.17 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 0.18 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.18 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.16 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.16 |
rpoB | 760658 | c.852G>A | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.18 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.16 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.15 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.15 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.14 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.15 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.18 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.14 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.13 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.14 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.15 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.17 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.16 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.16 |
rpoB | 760877 | c.1071G>C | synonymous_variant | 0.17 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.17 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.15 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.15 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.16 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.15 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.14 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.14 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.14 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.14 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.14 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.14 |
rpoB | 760949 | c.1143C>T | synonymous_variant | 0.14 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.16 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.16 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.16 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.16 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.16 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.15 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.16 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.17 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.16 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.14 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.15 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.16 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.18 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.19 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.18 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.18 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.2 |
rpoB | 761084 | c.1278C>T | synonymous_variant | 0.23 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.22 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.23 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.24 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.24 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.24 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.23 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.23 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.24 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.23 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.24 |
rpoB | 761198 | c.1392G>T | synonymous_variant | 0.23 |
rpoB | 761217 | p.Pro471Ala | missense_variant | 0.22 |
rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 0.22 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.23 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.24 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.22 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.21 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.14 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.14 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.13 |
rpoB | 762275 | c.2469C>A | synonymous_variant | 0.16 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.16 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.16 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.15 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.13 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.13 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.14 |
rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.14 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.16 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.18 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.18 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.18 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.19 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.19 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.18 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.18 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.18 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.17 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.18 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.2 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.25 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.25 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.23 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.22 |
rpoC | 763004 | c.-366G>A | upstream_gene_variant | 0.21 |
rpoC | 763007 | c.-363C>T | upstream_gene_variant | 0.2 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.23 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.24 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.23 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.24 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.22 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.19 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.2 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.19 |
rpoC | 763130 | c.-240G>A | upstream_gene_variant | 0.15 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.15 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.15 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.16 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.2 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.2 |
rpoC | 763558 | c.189C>T | synonymous_variant | 0.23 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.22 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.23 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.27 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.27 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.28 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.27 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.26 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.27 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.28 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.25 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.19 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.19 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.18 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.18 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.18 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.19 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.2 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.18 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.19 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.17 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.16 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.16 |
rpoC | 763813 | c.444C>G | synonymous_variant | 0.18 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.16 |
rpoC | 763837 | c.468G>C | synonymous_variant | 0.16 |
rpoC | 763840 | c.471G>C | synonymous_variant | 0.15 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.13 |
rpoC | 763921 | c.552G>C | synonymous_variant | 0.14 |
rpoC | 763924 | c.555G>A | synonymous_variant | 0.14 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.13 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.12 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.14 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.17 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.15 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.15 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.15 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.17 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.17 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.18 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.18 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.18 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.19 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.19 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.19 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.19 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.19 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.18 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.18 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.19 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.19 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.2 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.21 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.21 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.21 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.21 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.19 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.16 |
rpoC | 764707 | c.1338G>C | synonymous_variant | 0.14 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.14 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.14 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.15 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.16 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.16 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.16 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765871 | c.2502T>C | synonymous_variant | 0.13 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.13 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.14 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.13 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.13 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.13 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.13 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.14 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.14 |
rpoC | 765961 | c.2592G>T | synonymous_variant | 0.13 |
rpoC | 765964 | p.Leu865Phe | missense_variant | 0.13 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.13 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.13 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.13 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.13 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.12 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.13 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.13 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.14 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.15 |
rpoC | 767059 | c.3690T>C | synonymous_variant | 0.14 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.13 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.13 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.13 |
fbiC | 1304547 | c.1617C>G | synonymous_variant | 0.13 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.14 |
fbiC | 1304562 | c.1632G>C | synonymous_variant | 0.14 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.14 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.14 |
fbiC | 1304571 | c.1641G>C | synonymous_variant | 0.13 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.13 |
fbiC | 1304682 | c.1752C>T | synonymous_variant | 0.12 |
fbiC | 1305494 | c.2565_*55delGGCCTAGCCCCGGCGACGATGCCGGGTCGCGGGATGCGGCCCGTTGAGGAGCGGGGCAATCT | frameshift_variant&stop_lost&splice_region_variant | 0.26 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472286 | n.441C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472327 | n.482G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472328 | n.483G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472848 | n.1003T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472859 | n.1014G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474629 | n.972G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474710 | n.1053T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474711 | n.1054G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474712 | n.1055G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474713 | n.1056T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475602 | n.1945G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475603 | n.1946G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475604 | n.1947A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475612 | n.1955G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475615 | n.1958C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475616 | n.1959A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475618 | n.1961C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475629 | n.1972G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475637 | n.1980T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475638 | n.1981C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475643 | n.1986C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674477 | c.276G>T | synonymous_variant | 0.13 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.14 |
inhA | 1674503 | p.Thr101Ser | missense_variant | 0.14 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.15 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.14 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.15 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.15 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.16 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.16 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.16 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.19 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.18 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.21 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.21 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.21 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.21 |
rpsA | 1834330 | c.789C>G | synonymous_variant | 0.2 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.16 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.17 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.19 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.19 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.19 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.2 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.21 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.21 |
rpsA | 1834432 | c.891G>T | synonymous_variant | 0.23 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.23 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.23 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.22 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.2 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.2 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.2 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.18 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.18 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.17 |
rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 0.18 |
rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714432 | p.Val301Ile | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.99 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
rpoA | 3877803 | c.705G>C | synonymous_variant | 0.15 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.15 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.15 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.15 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.15 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.16 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.16 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.17 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.17 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.18 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.17 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.18 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.19 |
rpoA | 3877929 | c.579C>T | synonymous_variant | 0.19 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.22 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.19 |
rpoA | 3877974 | c.534G>T | synonymous_variant | 0.19 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.22 |
rpoA | 3877992 | c.516C>G | synonymous_variant | 0.21 |
rpoA | 3877998 | c.510G>C | synonymous_variant | 0.21 |
rpoA | 3878001 | c.505_507delTCAinsAGC | synonymous_variant | 0.2 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.21 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.21 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.21 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.22 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.21 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.22 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.23 |
rpoA | 3878050 | p.Arg153Lys | missense_variant | 0.22 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.21 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.22 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.21 |
rpoA | 3878079 | c.429C>T | synonymous_variant | 0.22 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.22 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.19 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.19 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.15 |
rpoA | 3878124 | c.384G>C | synonymous_variant | 0.14 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.14 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.16 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 0.17 |
rpoA | 3878154 | c.354G>C | synonymous_variant | 0.18 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.2 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.19 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.18 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.17 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.17 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.17 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.15 |
rpoA | 3878244 | c.264G>A | synonymous_variant | 0.14 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.14 |
rpoA | 3878639 | c.-132C>G | upstream_gene_variant | 0.17 |
rpoA | 3878641 | c.-135_-134insG | upstream_gene_variant | 0.17 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.13 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.15 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.14 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.15 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.14 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.15 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.15 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.16 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.17 |
clpC1 | 4039067 | c.1638G>T | synonymous_variant | 0.16 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.16 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.15 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.15 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.14 |
clpC1 | 4039100 | c.1605C>T | synonymous_variant | 0.15 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.15 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.15 |
clpC1 | 4039136 | c.1569C>T | synonymous_variant | 0.14 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.16 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.16 |
clpC1 | 4039169 | c.1536A>G | synonymous_variant | 0.16 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.14 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.14 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.14 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.13 |
clpC1 | 4039199 | c.1506C>G | synonymous_variant | 0.15 |
clpC1 | 4039241 | c.1464G>C | synonymous_variant | 0.15 |
clpC1 | 4039274 | c.1431G>A | synonymous_variant | 0.17 |
clpC1 | 4039277 | c.1428C>G | synonymous_variant | 0.15 |
clpC1 | 4039280 | c.1425G>C | synonymous_variant | 0.15 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.15 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.15 |
clpC1 | 4039295 | c.1410A>G | synonymous_variant | 0.14 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.13 |
clpC1 | 4039313 | c.1392C>G | synonymous_variant | 0.14 |
clpC1 | 4039321 | p.Ala462Ser | missense_variant | 0.12 |
clpC1 | 4039338 | p.Thr456Gln | missense_variant | 0.13 |
clpC1 | 4039346 | c.1359G>C | synonymous_variant | 0.13 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.13 |
clpC1 | 4039361 | c.1344C>A | synonymous_variant | 0.13 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.13 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.13 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.14 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.14 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.14 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.14 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.14 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.14 |
clpC1 | 4039598 | c.1107C>T | synonymous_variant | 0.17 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.17 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.17 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.15 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.15 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.16 |
clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.17 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.18 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.21 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.19 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.22 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.21 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.19 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.19 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.19 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.18 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.18 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.17 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.16 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.17 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 0.17 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.16 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.17 |
clpC1 | 4039829 | p.Leu292Phe | missense_variant | 0.14 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.12 |
clpC1 | 4039844 | c.861C>T | synonymous_variant | 0.13 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.13 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.14 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.13 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.13 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 0.14 |
clpC1 | 4040126 | c.579C>T | synonymous_variant | 0.16 |
clpC1 | 4040141 | c.564C>T | synonymous_variant | 0.13 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.13 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.13 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.14 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.14 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.14 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.14 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.14 |
clpC1 | 4040177 | c.528C>T | synonymous_variant | 0.16 |
clpC1 | 4040195 | c.510G>C | synonymous_variant | 0.16 |
clpC1 | 4040200 | c.505T>C | synonymous_variant | 0.17 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.16 |
clpC1 | 4040207 | c.498T>G | synonymous_variant | 0.15 |
clpC1 | 4040213 | p.Ser164Asn | missense_variant | 0.16 |
clpC1 | 4040219 | c.486C>G | synonymous_variant | 0.16 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.16 |
clpC1 | 4040228 | c.477G>A | synonymous_variant | 0.16 |
clpC1 | 4040231 | c.474C>T | synonymous_variant | 0.16 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.18 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.2 |
clpC1 | 4040258 | c.447G>A | synonymous_variant | 0.2 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.2 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.18 |
clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 0.17 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.17 |
clpC1 | 4040300 | c.405C>T | synonymous_variant | 0.17 |
clpC1 | 4040306 | c.399G>C | synonymous_variant | 0.15 |
embC | 4239763 | c.-100C>T | upstream_gene_variant | 0.99 |
embC | 4240382 | p.Gly174Arg | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
fbiC | 1305494 | c.2565_*56delCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN | frameshift_variant&stop_lost&splice_region_variant | 1.0 |