Run ID: ERR400538
Sample name:
Date: 01-04-2023 03:52:28
Number of reads: 1746642
Percentage reads mapped: 75.88
Strain: lineage5.1.2
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage5 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 0.98 |
lineage5.1.2 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Asp | missense_variant | 0.86 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.89 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.13 |
gyrA | 7006 | c.-296T>G | upstream_gene_variant | 0.14 |
gyrB | 7010 | p.Leu591Met | missense_variant | 0.13 |
gyrA | 7018 | c.-284G>C | upstream_gene_variant | 0.15 |
gyrA | 7024 | c.-278G>C | upstream_gene_variant | 0.17 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.2 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.18 |
gyrA | 7060 | c.-242T>C | upstream_gene_variant | 0.18 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.14 |
gyrA | 7078 | c.-224A>T | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7532 | c.231T>G | synonymous_variant | 0.19 |
gyrA | 7550 | c.249C>T | synonymous_variant | 0.21 |
gyrA | 7559 | c.258G>A | synonymous_variant | 0.2 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.21 |
gyrA | 7574 | c.273G>C | synonymous_variant | 0.21 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7587 | c.286C>T | synonymous_variant | 0.13 |
gyrA | 7595 | c.294C>T | synonymous_variant | 0.13 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.14 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.12 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.12 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.12 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.16 |
gyrA | 8924 | c.1623C>T | synonymous_variant | 0.2 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 0.19 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.18 |
gyrA | 8967 | p.Ala556Lys | missense_variant | 0.22 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.18 |
gyrA | 8993 | c.1692C>T | synonymous_variant | 0.17 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.17 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.18 |
gyrA | 9044 | c.1743C>G | synonymous_variant | 0.12 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9566 | c.2265C>T | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575756 | c.409C>T | synonymous_variant | 0.12 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.21 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.22 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.21 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.24 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.22 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.11 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.14 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.14 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.15 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.16 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.16 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.16 |
rpoB | 760412 | c.606C>T | synonymous_variant | 0.15 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.15 |
rpoB | 760418 | c.612G>A | synonymous_variant | 0.14 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.15 |
rpoB | 760433 | c.627C>T | synonymous_variant | 0.19 |
rpoB | 760454 | c.648C>G | synonymous_variant | 0.18 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.19 |
rpoB | 760469 | c.663C>T | synonymous_variant | 0.13 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.16 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.12 |
rpoB | 760541 | c.735G>T | synonymous_variant | 0.14 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.15 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.16 |
rpoB | 760588 | p.Thr261Ile | missense_variant | 0.15 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.15 |
rpoB | 760595 | c.789C>T | synonymous_variant | 0.14 |
rpoB | 760596 | p.Thr264Pro | missense_variant | 0.14 |
rpoB | 760607 | c.801G>C | synonymous_variant | 0.18 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.21 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.21 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.2 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.22 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.23 |
rpoB | 760668 | p.Thr288Ala | missense_variant | 0.22 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.21 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.2 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.17 |
rpoB | 760703 | c.897C>T | synonymous_variant | 0.16 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.11 |
rpoB | 760869 | p.Val355Leu | missense_variant | 0.12 |
rpoB | 760877 | c.1071G>C | synonymous_variant | 0.12 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.12 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.12 |
rpoB | 760887 | p.Thr361Ala | missense_variant | 0.12 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.17 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.15 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.17 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.14 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.14 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.17 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.16 |
rpoB | 761159 | c.1353G>T | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.13 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.13 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.13 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.2 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.15 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.14 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.13 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.13 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.15 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.15 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.16 |
rpoB | 761288 | c.1482G>T | synonymous_variant | 0.16 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.11 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.15 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.16 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.13 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.13 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.11 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.2 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.21 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.17 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.19 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.2 |
rpoB | 762056 | c.2250G>A | synonymous_variant | 0.2 |
rpoB | 762065 | c.2259T>G | synonymous_variant | 0.21 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.19 |
rpoB | 762086 | c.2280G>T | synonymous_variant | 0.19 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.16 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.12 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.13 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.11 |
rpoB | 762221 | c.2415G>A | synonymous_variant | 0.22 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.21 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.23 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.21 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.12 |
rpoC | 762894 | c.-476C>T | upstream_gene_variant | 0.12 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.11 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.16 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.15 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.13 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.13 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.15 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.16 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.15 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.16 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>A | upstream_gene_variant | 0.23 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.27 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.27 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.28 |
rpoC | 763085 | c.-285C>T | upstream_gene_variant | 0.29 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.29 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.28 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.23 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.14 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.2 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.21 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.27 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.3 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.36 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.3 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.21 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.22 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.19 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.16 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.12 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.13 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.16 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 0.18 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.19 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.18 |
rpoC | 764383 | c.1014C>T | synonymous_variant | 0.18 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.18 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.19 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.18 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.18 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.17 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.18 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.2 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.17 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.22 |
rpoC | 764506 | c.1137C>T | synonymous_variant | 0.22 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.13 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.14 |
rpoC | 764533 | c.1164C>A | synonymous_variant | 0.13 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.14 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.15 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.14 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.15 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.21 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.15 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.16 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.13 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.14 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.18 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.18 |
rpoC | 764635 | c.1266C>T | synonymous_variant | 0.17 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.12 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.27 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.31 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.33 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.33 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.33 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.32 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.28 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.28 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.23 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.19 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.17 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.18 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.18 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.19 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.2 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.22 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.22 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.22 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.21 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.18 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.14 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.14 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.14 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.14 |
rpoC | 765085 | c.1716T>C | synonymous_variant | 0.14 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.13 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.11 |
rpoC | 765394 | c.2025G>A | synonymous_variant | 0.15 |
rpoC | 765403 | c.2034G>C | synonymous_variant | 0.18 |
rpoC | 765405 | p.Leu679His | missense_variant | 0.17 |
rpoC | 765409 | c.2040T>G | synonymous_variant | 0.17 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.17 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.17 |
rpoC | 765449 | p.Ala694Ser | missense_variant | 0.13 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 0.13 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.14 |
rpoC | 765868 | c.2499G>A | synonymous_variant | 0.16 |
rpoC | 765871 | c.2502T>G | synonymous_variant | 0.15 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.2 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.19 |
rpoC | 765907 | c.2538G>T | synonymous_variant | 0.21 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.23 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.18 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.16 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.13 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.12 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.13 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.13 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.14 |
rpsL | 781670 | c.111G>C | synonymous_variant | 0.14 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.12 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.12 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.12 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.17 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.13 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.13 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.11 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303566 | c.636C>G | synonymous_variant | 0.13 |
Rv1258c | 1407273 | p.Asp23Val | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474181 | n.524_525insT | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474630 | n.973T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474743 | n.1086T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475061 | n.1406delA | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475954 | n.2297A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476295 | n.2638C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476311 | n.2654G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.15 |
inhA | 1673338 | c.-864G>A | upstream_gene_variant | 1.0 |
inhA | 1674114 | c.-88T>G | upstream_gene_variant | 0.14 |
inhA | 1674126 | c.-76G>C | upstream_gene_variant | 0.13 |
inhA | 1674129 | c.-73C>T | upstream_gene_variant | 0.13 |
inhA | 1674132 | c.-70T>C | upstream_gene_variant | 0.14 |
rpsA | 1833583 | c.42C>T | synonymous_variant | 0.16 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.14 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.14 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.14 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.16 |
rpsA | 1833616 | c.75A>T | synonymous_variant | 0.17 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.17 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.21 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.15 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.15 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.16 |
rpsA | 1833697 | c.156C>T | synonymous_variant | 0.16 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.17 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.17 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.13 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.12 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.19 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.19 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.15 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.15 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.17 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.15 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.16 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.13 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.14 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.13 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.13 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.14 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.16 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.23 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.2 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.21 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.21 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.15 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.14 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.17 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.17 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.18 |
rpsA | 1834033 | c.492C>T | synonymous_variant | 0.17 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.15 |
rpsA | 1834073 | p.Lys178Arg | missense_variant | 0.12 |
rpsA | 1834228 | c.687C>A | synonymous_variant | 0.14 |
rpsA | 1834231 | c.690T>G | synonymous_variant | 0.15 |
rpsA | 1834234 | c.693G>T | synonymous_variant | 0.15 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.15 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.16 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.17 |
rpsA | 1834252 | c.711C>G | synonymous_variant | 0.17 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.16 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.21 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.31 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.27 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.27 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.21 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.2 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.14 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.12 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.12 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.15 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.15 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.15 |
rpsA | 1834480 | c.939C>G | synonymous_variant | 0.12 |
rpsA | 1834483 | c.942G>A | synonymous_variant | 0.13 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.17 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.19 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.18 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.19 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.13 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.12 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.13 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.15 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.13 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.13 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.14 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.2 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.21 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.17 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.17 |
rpsA | 1834684 | c.1143C>G | synonymous_variant | 0.14 |
rpsA | 1834701 | p.Gln387Pro | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101921 | c.1122G>A | synonymous_variant | 1.0 |
ndh | 2103112 | c.-70G>T | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170265 | c.347delG | frameshift_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290062 | c.-821G>A | upstream_gene_variant | 0.97 |
kasA | 2517917 | c.-198G>C | upstream_gene_variant | 0.17 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726261 | c.69G>T | synonymous_variant | 1.0 |
thyA | 3073950 | c.522G>T | synonymous_variant | 0.13 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.12 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.12 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
ald | 3087184 | c.368_373delCCGACG | disruptive_inframe_deletion | 1.0 |
Rv3083 | 3449644 | p.Ala381Thr | missense_variant | 1.0 |
Rv3083 | 3449792 | p.Ala430Gly | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiB | 3641490 | c.-45G>A | upstream_gene_variant | 1.0 |
alr | 3840932 | c.489C>T | synonymous_variant | 1.0 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.16 |
rpoA | 3877596 | c.912G>C | synonymous_variant | 0.19 |
rpoA | 3877602 | c.906C>T | synonymous_variant | 0.18 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.16 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 0.16 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.16 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.17 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 0.13 |
rpoA | 3877680 | c.828G>T | synonymous_variant | 0.13 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.13 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.13 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.15 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.16 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.2 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.21 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.19 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.2 |
rpoA | 3877758 | c.750G>C | synonymous_variant | 0.21 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.17 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.17 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 0.19 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.19 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.19 |
rpoA | 3877785 | c.723C>A | synonymous_variant | 0.19 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.17 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.12 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.12 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.15 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.14 |
rpoA | 3877900 | p.Ser203Thr | missense_variant | 0.14 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.15 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.14 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.14 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.13 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.14 |
rpoA | 3877929 | p.Ile193Val | missense_variant | 0.14 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.11 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.11 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.12 |
rpoA | 3878205 | c.303T>A | synonymous_variant | 0.14 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.18 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.17 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.11 |
rpoA | 3878274 | c.234G>C | synonymous_variant | 0.12 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.1 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.12 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.12 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.12 |
rpoA | 3878373 | c.135G>C | synonymous_variant | 0.12 |
rpoA | 3878391 | c.117T>G | synonymous_variant | 0.14 |
rpoA | 3878400 | c.108T>C | synonymous_variant | 0.12 |
rpoA | 3878493 | c.15G>A | synonymous_variant | 1.0 |
ddn | 3986987 | c.144G>T | synonymous_variant | 1.0 |
ddn | 3987180 | p.Asp113Asn | missense_variant | 1.0 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.12 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 0.14 |
clpC1 | 4038860 | c.1845G>T | synonymous_variant | 0.25 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.2 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.14 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.13 |
clpC1 | 4039031 | c.1674T>C | synonymous_variant | 0.14 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.15 |
clpC1 | 4039070 | c.1635G>C | synonymous_variant | 0.12 |
clpC1 | 4039136 | c.1569C>T | synonymous_variant | 0.12 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.12 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.11 |
clpC1 | 4039166 | c.1539G>A | synonymous_variant | 0.12 |
clpC1 | 4039169 | c.1536A>G | synonymous_variant | 0.12 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.14 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.14 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.15 |
clpC1 | 4039190 | c.1515C>T | synonymous_variant | 0.15 |
clpC1 | 4039196 | c.1509G>A | synonymous_variant | 0.15 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.16 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.18 |
clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.21 |
clpC1 | 4039238 | c.1467C>T | synonymous_variant | 0.22 |
clpC1 | 4039265 | c.1440C>T | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.15 |
clpC1 | 4039277 | c.1428C>G | synonymous_variant | 0.17 |
clpC1 | 4039280 | c.1425G>T | synonymous_variant | 0.14 |
clpC1 | 4039283 | c.1422C>T | synonymous_variant | 0.13 |
clpC1 | 4039286 | c.1419T>G | synonymous_variant | 0.14 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.19 |
clpC1 | 4039316 | p.Glu463Asp | missense_variant | 0.15 |
clpC1 | 4039319 | c.1386T>A | synonymous_variant | 0.15 |
clpC1 | 4039322 | c.1383T>G | synonymous_variant | 0.14 |
clpC1 | 4039360 | p.Ser449Arg | missense_variant | 0.15 |
clpC1 | 4039361 | c.1344C>G | synonymous_variant | 0.15 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.18 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.16 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.21 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.24 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.31 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.32 |
clpC1 | 4039451 | c.1254G>A | synonymous_variant | 0.28 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.3 |
clpC1 | 4039457 | c.1248C>T | synonymous_variant | 0.27 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.19 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.19 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.19 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.21 |
clpC1 | 4039478 | c.1227G>C | synonymous_variant | 0.19 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.18 |
clpC1 | 4039484 | c.1221T>A | synonymous_variant | 0.19 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.17 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.11 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.11 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.12 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.12 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.15 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.18 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.22 |
clpC1 | 4039610 | c.1095G>T | synonymous_variant | 0.22 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.26 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.24 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.22 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.23 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.27 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.29 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.26 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.24 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.24 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.2 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.18 |
clpC1 | 4039769 | c.936C>T | synonymous_variant | 0.24 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.23 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.24 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.21 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.19 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.18 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.18 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.18 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.16 |
clpC1 | 4039844 | c.861C>T | synonymous_variant | 0.12 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.12 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.12 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.11 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.12 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.12 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.12 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.19 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.22 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.24 |
clpC1 | 4039975 | p.Asp244Asn | missense_variant | 0.21 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.19 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.16 |
clpC1 | 4040000 | c.705C>T | synonymous_variant | 0.15 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.22 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.23 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.29 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.22 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.15 |
clpC1 | 4040090 | p.Ser205Cys | missense_variant | 0.11 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.12 |
clpC1 | 4040824 | c.-120C>T | upstream_gene_variant | 1.0 |
embC | 4239843 | c.-20A>C | upstream_gene_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244635 | p.Val468Ala | missense_variant | 1.0 |
embA | 4245147 | p.Pro639Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethR | 4326928 | c.-621G>A | upstream_gene_variant | 1.0 |
ethA | 4327103 | p.Gly124Asp | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |