Run ID: ERR9901856
Sample name:
Date: 02-04-2023 13:33:43
Number of reads: 295072
Percentage reads mapped: 99.12
Strain: lineage1.1.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsA | 1834962 | p.Arg474Leu | missense_variant | 0.18 | pyrazinamide |
tlyA | 1917991 | p.Arg18* | stop_gained | 0.29 | capreomycin |
katG | 2155193 | p.Gly307Arg | missense_variant | 0.18 | isoniazid |
pncA | 2289073 | p.His57Asn | missense_variant | 0.18 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5660 | p.Arg141Ser | missense_variant | 0.17 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrA | 6904 | c.-398C>A | upstream_gene_variant | 0.22 |
gyrB | 7118 | p.Asp627Tyr | missense_variant | 0.17 |
gyrA | 7153 | c.-149G>T | upstream_gene_variant | 0.29 |
gyrA | 7264 | c.-38C>A | upstream_gene_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7961 | p.Met220Ile | missense_variant | 0.25 |
gyrA | 8400 | p.Asp367Tyr | missense_variant | 0.18 |
gyrA | 8406 | p.Gln369Lys | missense_variant | 0.36 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8577 | p.Asp426Tyr | missense_variant | 0.2 |
gyrA | 8607 | p.Leu436Met | missense_variant | 0.22 |
gyrA | 8649 | p.Arg450Cys | missense_variant | 0.29 |
gyrA | 8763 | p.Asp488Tyr | missense_variant | 0.29 |
gyrA | 8922 | p.Gly541Cys | missense_variant | 0.25 |
gyrA | 8936 | p.Gln545His | missense_variant | 0.17 |
gyrA | 8958 | p.Asp553Tyr | missense_variant | 0.22 |
gyrA | 9058 | p.Glu586Ala | missense_variant | 0.13 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9215 | c.1914C>A | synonymous_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9350 | p.Phe683Leu | missense_variant | 0.2 |
gyrA | 9359 | c.2058C>A | synonymous_variant | 0.22 |
gyrA | 9536 | c.2235C>T | synonymous_variant | 0.22 |
gyrA | 9560 | c.2259C>A | synonymous_variant | 0.25 |
gyrA | 9768 | p.Gly823Cys | missense_variant | 0.29 |
gyrA | 9785 | c.2484G>T | synonymous_variant | 0.22 |
fgd1 | 490676 | c.-107G>A | upstream_gene_variant | 0.2 |
fgd1 | 490815 | c.33G>T | synonymous_variant | 0.29 |
fgd1 | 490870 | p.His30Asn | missense_variant | 0.25 |
fgd1 | 490993 | p.Gly71Cys | missense_variant | 0.17 |
fgd1 | 491132 | p.Gly117Val | missense_variant | 0.18 |
fgd1 | 491139 | p.Glu119Asp | missense_variant | 0.55 |
fgd1 | 491256 | p.Lys158Asn | missense_variant | 0.33 |
fgd1 | 491307 | c.525C>A | synonymous_variant | 0.4 |
fgd1 | 491325 | c.543G>T | synonymous_variant | 0.29 |
fgd1 | 491485 | p.Tyr235His | missense_variant | 0.25 |
fgd1 | 491493 | c.713_724delACCCGGAGCTGG | disruptive_inframe_deletion | 0.4 |
fgd1 | 491575 | p.Pro265Thr | missense_variant | 0.2 |
fgd1 | 491581 | p.Glu267* | stop_gained | 0.2 |
fgd1 | 491704 | p.Leu308Met | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575188 | c.-160G>T | upstream_gene_variant | 0.18 |
mshA | 575378 | p.Gly11Trp | missense_variant | 0.2 |
mshA | 575745 | p.Ala133Asp | missense_variant | 0.33 |
mshA | 575773 | c.426C>A | synonymous_variant | 0.4 |
mshA | 575831 | p.Gly162Cys | missense_variant | 0.33 |
mshA | 575951 | p.Gly202Trp | missense_variant | 0.25 |
mshA | 576246 | p.Gly300Val | missense_variant | 0.4 |
mshA | 576278 | p.Gly311* | stop_gained | 0.33 |
mshA | 576394 | c.1047G>T | synonymous_variant | 0.2 |
mshA | 576484 | c.1137C>A | synonymous_variant | 0.2 |
mshA | 576520 | c.1173C>A | synonymous_variant | 0.2 |
mshA | 576577 | c.1230C>A | synonymous_variant | 0.29 |
mshA | 576758 | p.His471Asn | missense_variant | 0.29 |
ccsA | 619754 | c.-137C>A | upstream_gene_variant | 0.5 |
ccsA | 619789 | c.-102G>T | upstream_gene_variant | 0.29 |
ccsA | 619802 | c.-89G>T | upstream_gene_variant | 0.29 |
ccsA | 620008 | p.Arg40Ser | missense_variant | 0.33 |
ccsA | 620155 | p.Gly89Trp | missense_variant | 0.33 |
ccsA | 620175 | c.285C>A | synonymous_variant | 0.25 |
ccsA | 620249 | p.Ser120Tyr | missense_variant | 0.18 |
ccsA | 620251 | p.Gly121Trp | missense_variant | 0.18 |
ccsA | 620263 | p.Gly125Cys | missense_variant | 0.2 |
ccsA | 620319 | c.429C>A | synonymous_variant | 0.2 |
ccsA | 620563 | p.Leu225Met | missense_variant | 0.31 |
ccsA | 620603 | p.Pro238His | missense_variant | 0.31 |
rpoB | 760250 | p.Met148Ile | missense_variant | 0.2 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoB | 760604 | p.Glu266Asp | missense_variant | 0.17 |
rpoB | 760640 | c.834C>A | synonymous_variant | 0.17 |
rpoB | 760768 | p.Pro321His | missense_variant | 0.18 |
rpoB | 760838 | p.Glu344Asp | missense_variant | 0.25 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.25 |
rpoB | 761129 | c.1323G>T | synonymous_variant | 0.29 |
rpoB | 761212 | p.Val469Glu | missense_variant | 0.2 |
rpoB | 761218 | p.Pro471Gln | missense_variant | 0.2 |
rpoB | 761233 | p.Arg476Leu | missense_variant | 0.2 |
rpoB | 761240 | p.Cys478* | stop_gained | 0.18 |
rpoB | 761787 | c.1981C>A | synonymous_variant | 0.29 |
rpoB | 761821 | p.Ser672Tyr | missense_variant | 0.25 |
rpoB | 762109 | p.Pro768Gln | missense_variant | 0.4 |
rpoB | 762164 | c.2358C>A | synonymous_variant | 0.29 |
rpoB | 762825 | p.Gly1007Trp | missense_variant | 0.33 |
rpoC | 762959 | c.-411G>T | upstream_gene_variant | 0.22 |
rpoB | 762963 | p.Gly1053Cys | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763785 | p.Val139Ala | missense_variant | 0.15 |
rpoC | 763834 | p.Met155Ile | missense_variant | 0.25 |
rpoC | 763841 | p.Glu158* | stop_gained | 0.25 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 763986 | p.Arg206His | missense_variant | 0.22 |
rpoC | 764021 | c.652C>A | synonymous_variant | 0.18 |
rpoC | 764062 | c.693C>A | synonymous_variant | 0.19 |
rpoC | 764128 | c.759C>A | synonymous_variant | 0.18 |
rpoC | 764243 | c.877delC | frameshift_variant | 0.11 |
rpoC | 764443 | c.1074C>A | synonymous_variant | 0.2 |
rpoC | 764693 | p.Gly442Cys | missense_variant | 0.2 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.22 |
rpoC | 764730 | p.Pro454Gln | missense_variant | 0.22 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.22 |
rpoC | 765145 | c.1776C>A | synonymous_variant | 0.4 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765210 | p.Ser614* | stop_gained | 0.22 |
rpoC | 765483 | p.Pro705Gln | missense_variant | 0.22 |
rpoC | 765508 | c.2139C>A | synonymous_variant | 0.67 |
rpoC | 765604 | c.2235C>A | synonymous_variant | 0.25 |
rpoC | 765656 | p.Gly763Cys | missense_variant | 0.25 |
rpoC | 765683 | p.Glu772* | stop_gained | 0.2 |
rpoC | 765738 | p.Arg790Leu | missense_variant | 0.29 |
rpoC | 765805 | c.2436C>A | synonymous_variant | 0.29 |
rpoC | 765813 | p.Arg815Gln | missense_variant | 0.29 |
rpoC | 766038 | p.Asp890Val | missense_variant | 0.33 |
rpoC | 766105 | c.2736C>A | synonymous_variant | 0.33 |
rpoC | 766511 | p.Asp1048Tyr | missense_variant | 0.22 |
rpoC | 766588 | p.Glu1073Asp | missense_variant | 0.17 |
rpoC | 766864 | c.3495G>T | synonymous_variant | 0.31 |
rpoC | 766951 | c.3582G>T | synonymous_variant | 0.25 |
rpoC | 766952 | p.Ala1195Ser | missense_variant | 0.25 |
rpoC | 766964 | p.Glu1199* | stop_gained | 0.25 |
rpoC | 766968 | p.Pro1200His | missense_variant | 0.25 |
rpoC | 767309 | p.Asp1314Tyr | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776323 | p.Ile720Val | missense_variant | 0.22 |
mmpL5 | 776344 | p.Gly713Trp | missense_variant | 0.29 |
mmpL5 | 776371 | p.Gly704Cys | missense_variant | 0.25 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
mmpL5 | 776468 | p.Glu671Asp | missense_variant | 0.29 |
mmpL5 | 776500 | p.Gly661Trp | missense_variant | 0.17 |
mmpL5 | 776584 | p.Gln633Lys | missense_variant | 0.22 |
mmpL5 | 776785 | p.Glu566* | stop_gained | 0.18 |
mmpL5 | 776807 | c.1674G>T | synonymous_variant | 0.29 |
mmpL5 | 776810 | p.Met557Ile | missense_variant | 0.29 |
mmpL5 | 777263 | c.1218G>T | synonymous_variant | 0.29 |
mmpL5 | 777425 | c.1056C>A | synonymous_variant | 0.67 |
mmpL5 | 777907 | p.Leu192Met | missense_variant | 0.18 |
mmpR5 | 777998 | c.-992C>A | upstream_gene_variant | 0.29 |
mmpL5 | 778018 | p.Gly155Cys | missense_variant | 0.22 |
mmpL5 | 778276 | p.Ala69Ser | missense_variant | 0.14 |
mmpS5 | 778646 | p.Pro87Gln | missense_variant | 0.22 |
mmpL5 | 778963 | c.-483G>T | upstream_gene_variant | 0.25 |
mmpL5 | 779049 | c.-569G>T | upstream_gene_variant | 0.4 |
mmpL5 | 779101 | c.-621G>T | upstream_gene_variant | 0.25 |
mmpS5 | 779675 | c.-770G>T | upstream_gene_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781861 | p.Ser101* | stop_gained | 0.25 |
rpsL | 781895 | p.Gln112His | missense_variant | 0.25 |
rplC | 800708 | c.-101C>A | upstream_gene_variant | 0.22 |
rplC | 800767 | c.-42C>A | upstream_gene_variant | 0.18 |
rplC | 800799 | c.-10G>T | upstream_gene_variant | 0.2 |
rplC | 801100 | p.Gly98Trp | missense_variant | 0.18 |
rplC | 801145 | p.Asp113Tyr | missense_variant | 0.4 |
rplC | 801252 | c.444G>T | synonymous_variant | 0.2 |
fbiC | 1303091 | p.Glu54Val | missense_variant | 0.2 |
fbiC | 1303548 | c.618G>T | synonymous_variant | 0.2 |
fbiC | 1303686 | c.756C>A | synonymous_variant | 0.18 |
fbiC | 1303713 | c.783C>A | synonymous_variant | 0.2 |
fbiC | 1303979 | p.Gly350Val | missense_variant | 0.17 |
fbiC | 1304475 | c.1545G>T | synonymous_variant | 0.5 |
fbiC | 1304547 | c.1617C>A | synonymous_variant | 0.5 |
fbiC | 1304790 | c.1860C>A | synonymous_variant | 0.18 |
fbiC | 1304825 | p.Ala632Glu | missense_variant | 0.33 |
fbiC | 1304834 | p.Pro635Gln | missense_variant | 0.33 |
fbiC | 1304871 | c.1941G>T | synonymous_variant | 0.2 |
fbiC | 1304902 | p.Glu658* | stop_gained | 0.2 |
fbiC | 1305018 | c.2088C>A | synonymous_variant | 0.18 |
fbiC | 1305108 | c.2178G>T | synonymous_variant | 0.22 |
fbiC | 1305458 | p.Pro843Gln | missense_variant | 0.22 |
Rv1258c | 1406361 | p.Pro327His | missense_variant | 0.33 |
Rv1258c | 1406376 | p.Gly322Val | missense_variant | 0.25 |
Rv1258c | 1406515 | p.Leu276Met | missense_variant | 0.29 |
Rv1258c | 1406709 | p.Gly211Val | missense_variant | 0.25 |
Rv1258c | 1406725 | p.Gln206Lys | missense_variant | 0.4 |
Rv1258c | 1406928 | p.Ser138* | stop_gained | 0.2 |
Rv1258c | 1407072 | p.Pro90His | missense_variant | 0.29 |
Rv1258c | 1407116 | p.Ser75Tyr | missense_variant | 0.22 |
Rv1258c | 1407133 | p.Gly70Trp | missense_variant | 0.18 |
embR | 1416539 | p.Ala270Asp | missense_variant | 0.15 |
embR | 1416742 | c.606C>A | synonymous_variant | 0.22 |
embR | 1416829 | c.519C>G | synonymous_variant | 0.67 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417030 | c.318C>A | synonymous_variant | 0.29 |
embR | 1417079 | p.Pro90Gln | missense_variant | 0.25 |
embR | 1417113 | p.Leu79Met | missense_variant | 0.29 |
embR | 1417131 | p.His73Asn | missense_variant | 0.22 |
embR | 1417164 | p.Glu62* | stop_gained | 0.18 |
embR | 1417173 | p.Leu59Ile | missense_variant | 0.27 |
embR | 1417186 | c.162C>A | synonymous_variant | 0.22 |
embR | 1417400 | c.-53C>T | upstream_gene_variant | 0.2 |
embR | 1417403 | c.-56G>T | upstream_gene_variant | 0.2 |
embR | 1417477 | c.-130C>A | upstream_gene_variant | 0.33 |
embR | 1417484 | c.-137C>A | upstream_gene_variant | 0.25 |
embR | 1417522 | c.-175C>A | upstream_gene_variant | 0.2 |
atpE | 1461051 | p.Pro3Thr | missense_variant | 0.2 |
atpE | 1461145 | p.Ala34Glu | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472745 | n.900A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472765 | n.920G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474841 | n.1184G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474842 | n.1185G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474923 | n.1266G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475034 | n.1377G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475097 | n.1440G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475102 | n.1445C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475262 | n.1605G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476265 | n.2608G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476337 | n.2680C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476777 | n.3120C>A | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673192 | c.-248C>A | upstream_gene_variant | 0.18 |
fabG1 | 1673361 | c.-79C>A | upstream_gene_variant | 0.29 |
fabG1 | 1673375 | c.-65A>G | upstream_gene_variant | 0.22 |
fabG1 | 1673504 | p.Gly22Val | missense_variant | 0.25 |
fabG1 | 1673587 | p.Gly50* | stop_gained | 0.29 |
inhA | 1673640 | c.-562C>A | upstream_gene_variant | 0.22 |
fabG1 | 1673646 | p.Asp69Glu | missense_variant | 0.2 |
fabG1 | 1673828 | p.Asn130Ser | missense_variant | 0.18 |
fabG1 | 1673936 | p.Ser166* | stop_gained | 0.33 |
inhA | 1673991 | c.-211C>A | upstream_gene_variant | 0.29 |
fabG1 | 1674040 | p.Gly201Trp | missense_variant | 0.25 |
inhA | 1674469 | p.Gly90Trp | missense_variant | 0.3 |
inhA | 1674693 | c.492C>A | synonymous_variant | 0.18 |
inhA | 1674750 | c.549T>C | synonymous_variant | 0.14 |
inhA | 1674861 | p.Glu220Asp | missense_variant | 0.2 |
inhA | 1674880 | p.Pro227Thr | missense_variant | 0.2 |
inhA | 1674918 | c.717C>A | synonymous_variant | 0.33 |
inhA | 1674959 | p.Thr253Asn | missense_variant | 0.25 |
rpsA | 1833432 | c.-110C>A | upstream_gene_variant | 0.18 |
rpsA | 1833514 | c.-28C>A | upstream_gene_variant | 0.33 |
rpsA | 1834175 | c.634C>A | synonymous_variant | 0.22 |
rpsA | 1834192 | c.651C>A | synonymous_variant | 0.22 |
rpsA | 1834194 | p.Ser218* | stop_gained | 0.29 |
rpsA | 1834256 | p.Glu239* | stop_gained | 0.33 |
rpsA | 1834349 | p.Glu270* | stop_gained | 0.18 |
rpsA | 1834385 | p.Asp282Tyr | missense_variant | 0.17 |
rpsA | 1834435 | c.894G>T | synonymous_variant | 0.22 |
rpsA | 1834462 | p.Phe307Leu | missense_variant | 0.33 |
rpsA | 1834870 | c.1329C>T | synonymous_variant | 0.25 |
tlyA | 1917776 | c.-164G>T | upstream_gene_variant | 0.25 |
tlyA | 1917786 | c.-154G>A | upstream_gene_variant | 0.25 |
tlyA | 1917839 | c.-101_-100insC | upstream_gene_variant | 0.5 |
tlyA | 1917891 | c.-49G>T | upstream_gene_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918285 | p.Gly116Cys | missense_variant | 0.22 |
tlyA | 1918326 | c.387G>T | synonymous_variant | 0.2 |
tlyA | 1918387 | p.Leu150Met | missense_variant | 0.18 |
tlyA | 1918402 | p.Leu155Met | missense_variant | 0.18 |
tlyA | 1918621 | p.Ser228Gly | missense_variant | 0.11 |
tlyA | 1918737 | p.Glu266Asp | missense_variant | 0.18 |
ndh | 2101679 | p.Ser455* | stop_gained | 0.25 |
ndh | 2101717 | c.1326C>A | synonymous_variant | 0.25 |
ndh | 2102065 | c.978G>T | synonymous_variant | 0.22 |
ndh | 2102121 | p.Asp308Tyr | missense_variant | 0.22 |
ndh | 2102138 | p.Arg302Leu | missense_variant | 0.2 |
ndh | 2102172 | p.Glu291* | stop_gained | 0.25 |
ndh | 2102292 | p.Asp251Tyr | missense_variant | 0.29 |
ndh | 2102293 | c.750C>A | synonymous_variant | 0.29 |
ndh | 2102766 | p.Asp93Tyr | missense_variant | 0.33 |
ndh | 2102830 | c.213G>T | synonymous_variant | 0.18 |
ndh | 2102944 | c.99C>A | synonymous_variant | 0.18 |
ndh | 2102971 | p.Phe24Leu | missense_variant | 0.22 |
ndh | 2103023 | p.Pro7His | missense_variant | 0.33 |
ndh | 2103033 | p.Gln4Lys | missense_variant | 0.33 |
ndh | 2103131 | c.-89C>A | upstream_gene_variant | 0.17 |
ndh | 2103242 | c.-200A>G | upstream_gene_variant | 0.33 |
katG | 2153909 | p.Asp735Tyr | missense_variant | 0.18 |
katG | 2153945 | p.Asp723Tyr | missense_variant | 0.18 |
katG | 2153999 | p.Arg705Trp | missense_variant | 0.2 |
katG | 2154030 | c.2082G>T | synonymous_variant | 0.18 |
katG | 2154034 | p.Arg693Leu | missense_variant | 0.18 |
katG | 2154150 | c.1962C>A | synonymous_variant | 0.67 |
katG | 2154212 | p.Leu634Ile | missense_variant | 0.29 |
katG | 2154414 | c.1698C>A | synonymous_variant | 0.18 |
katG | 2154564 | p.Lys516Asn | missense_variant | 0.17 |
katG | 2154577 | p.Gly512Val | missense_variant | 0.2 |
katG | 2154598 | p.Trp505Leu | missense_variant | 0.25 |
katG | 2154723 | p.Arg463Leu | missense_variant | 0.33 |
katG | 2154761 | p.Gly451Ser | missense_variant | 0.25 |
katG | 2154938 | p.Arg392Trp | missense_variant | 0.22 |
katG | 2155018 | p.Pro365Gln | missense_variant | 0.25 |
katG | 2155090 | p.Trp341Leu | missense_variant | 0.17 |
katG | 2155177 | p.Ala312Glu | missense_variant | 0.17 |
katG | 2155254 | c.858C>A | synonymous_variant | 0.25 |
katG | 2155471 | p.Arg214Leu | missense_variant | 0.18 |
katG | 2155662 | c.450G>A | synonymous_variant | 0.22 |
katG | 2155816 | p.Gly99Val | missense_variant | 0.5 |
katG | 2155871 | p.Glu81* | stop_gained | 0.5 |
katG | 2156106 | c.6C>A | synonymous_variant | 0.22 |
katG | 2156123 | c.-12G>T | upstream_gene_variant | 0.25 |
katG | 2156341 | c.-230G>T | upstream_gene_variant | 0.25 |
katG | 2156488 | c.-377C>A | upstream_gene_variant | 0.25 |
katG | 2156536 | c.-425C>A | upstream_gene_variant | 0.22 |
PPE35 | 2167666 | p.Gln983Lys | missense_variant | 0.25 |
PPE35 | 2167679 | c.2934G>T | synonymous_variant | 0.2 |
PPE35 | 2167790 | p.Ser941* | stop_gained | 0.25 |
PPE35 | 2167801 | p.Gly938Cys | missense_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2168021 | c.2592C>A | synonymous_variant | 0.18 |
PPE35 | 2168186 | c.2427C>T | synonymous_variant | 0.18 |
PPE35 | 2168189 | c.2424T>G | synonymous_variant | 0.18 |
PPE35 | 2168222 | c.2391G>T | synonymous_variant | 0.25 |
PPE35 | 2168275 | p.Thr780Ala | missense_variant | 0.14 |
PPE35 | 2169827 | c.786G>T | synonymous_variant | 0.21 |
PPE35 | 2169970 | p.Gly215Cys | missense_variant | 0.33 |
PPE35 | 2169976 | p.Gly213Cys | missense_variant | 0.33 |
PPE35 | 2170097 | c.516G>T | synonymous_variant | 0.33 |
PPE35 | 2170150 | p.His155Asn | missense_variant | 0.22 |
PPE35 | 2170373 | c.240G>T | synonymous_variant | 0.4 |
PPE35 | 2170424 | c.189G>T | synonymous_variant | 0.67 |
PPE35 | 2170450 | p.Gly55Trp | missense_variant | 0.4 |
PPE35 | 2170548 | p.Gly22Val | missense_variant | 0.17 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222571 | c.594G>A | synonymous_variant | 1.0 |
Rv1979c | 2223093 | c.72C>A | synonymous_variant | 0.2 |
Rv1979c | 2223249 | c.-85G>T | upstream_gene_variant | 0.25 |
Rv1979c | 2223275 | c.-111C>A | upstream_gene_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288702 | c.540C>A | synonymous_variant | 0.22 |
pncA | 2288903 | c.339C>T | synonymous_variant | 0.22 |
pncA | 2289012 | p.Pro77His | missense_variant | 0.18 |
pncA | 2289197 | p.Glu15Asp | missense_variant | 0.17 |
pncA | 2289267 | c.-26C>A | upstream_gene_variant | 0.14 |
pncA | 2289448 | c.-207G>T | upstream_gene_variant | 0.18 |
pncA | 2289460 | c.-219G>T | upstream_gene_variant | 0.18 |
pncA | 2289505 | c.-264G>T | upstream_gene_variant | 0.5 |
pncA | 2289626 | c.-385G>T | upstream_gene_variant | 0.22 |
pncA | 2289815 | c.-574C>A | upstream_gene_variant | 0.18 |
kasA | 2517948 | c.-167C>A | upstream_gene_variant | 0.17 |
kasA | 2518039 | c.-76C>A | upstream_gene_variant | 0.33 |
kasA | 2518069 | c.-46C>A | upstream_gene_variant | 0.2 |
kasA | 2518075 | c.-40C>T | upstream_gene_variant | 0.2 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518177 | c.63G>T | synonymous_variant | 0.25 |
kasA | 2518363 | c.249C>A | synonymous_variant | 0.33 |
kasA | 2518659 | p.Trp182Leu | missense_variant | 0.67 |
kasA | 2518716 | p.Pro201His | missense_variant | 0.33 |
kasA | 2518945 | p.Met277Ile | missense_variant | 0.33 |
kasA | 2519113 | p.Gln333His | missense_variant | 0.17 |
kasA | 2519178 | p.Ser355Leu | missense_variant | 0.25 |
eis | 2714505 | c.828C>A | synonymous_variant | 0.18 |
eis | 2714525 | p.His270Asn | missense_variant | 0.2 |
eis | 2714795 | p.Glu180* | stop_gained | 0.21 |
eis | 2714928 | c.405C>A | synonymous_variant | 0.15 |
eis | 2715182 | p.Gly51Cys | missense_variant | 0.18 |
eis | 2715238 | p.Ser32* | stop_gained | 0.2 |
eis | 2715525 | c.-193G>T | upstream_gene_variant | 0.25 |
ahpC | 2725978 | c.-215G>T | upstream_gene_variant | 0.27 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726225 | c.33C>A | synonymous_variant | 0.25 |
ahpC | 2726611 | p.Pro140His | missense_variant | 0.22 |
ahpC | 2726732 | p.Lys180Asn | missense_variant | 0.22 |
folC | 2746163 | p.Arg479Leu | missense_variant | 0.29 |
folC | 2746227 | p.Gly458Trp | missense_variant | 0.33 |
folC | 2746270 | c.1329C>A | synonymous_variant | 0.25 |
folC | 2746313 | p.Arg429Leu | missense_variant | 0.33 |
folC | 2746387 | c.1212C>A | synonymous_variant | 0.5 |
folC | 2746438 | c.1161G>T | synonymous_variant | 0.4 |
folC | 2746453 | c.1146G>T | synonymous_variant | 0.29 |
folC | 2746469 | p.Gly377Val | missense_variant | 0.29 |
folC | 2746523 | p.Ala359Glu | missense_variant | 0.15 |
folC | 2746587 | c.1012C>A | synonymous_variant | 0.2 |
folC | 2746876 | c.723C>A | synonymous_variant | 0.67 |
folC | 2746923 | p.Gly226Cys | missense_variant | 0.43 |
folC | 2746933 | c.666G>T | synonymous_variant | 0.25 |
folC | 2746947 | p.Gly218Cys | missense_variant | 0.22 |
folC | 2746956 | p.Glu215* | stop_gained | 0.22 |
folC | 2747012 | p.Pro196Gln | missense_variant | 0.2 |
folC | 2747030 | p.Pro190Gln | missense_variant | 0.25 |
folC | 2747041 | c.558G>T | synonymous_variant | 0.2 |
folC | 2747057 | p.Trp181Leu | missense_variant | 0.29 |
folC | 2747113 | p.Ala162Glu | missense_variant | 0.2 |
folC | 2747272 | c.327G>T | synonymous_variant | 0.25 |
folC | 2747324 | p.Arg92Leu | missense_variant | 0.2 |
folC | 2747419 | c.180C>A | synonymous_variant | 0.27 |
folC | 2747566 | c.33G>T | synonymous_variant | 0.4 |
folC | 2747643 | c.-45G>T | upstream_gene_variant | 0.4 |
pepQ | 2859746 | p.Leu225Met | missense_variant | 0.29 |
pepQ | 2859776 | p.Gly215Cys | missense_variant | 0.29 |
pepQ | 2859777 | c.642C>A | synonymous_variant | 0.29 |
pepQ | 2859872 | p.His183Asn | missense_variant | 0.33 |
pepQ | 2859885 | c.534C>A | synonymous_variant | 0.22 |
pepQ | 2860177 | p.Arg81Leu | missense_variant | 0.18 |
pepQ | 2860189 | p.Arg77Leu | missense_variant | 0.25 |
pepQ | 2860212 | c.207C>A | synonymous_variant | 0.4 |
pepQ | 2860287 | c.132G>A | synonymous_variant | 0.29 |
pepQ | 2860423 | c.-5G>T | upstream_gene_variant | 0.2 |
ribD | 2986702 | c.-137G>T | upstream_gene_variant | 0.25 |
ribD | 2986745 | c.-94C>A | upstream_gene_variant | 0.22 |
ribD | 2986765 | c.-74G>T | upstream_gene_variant | 0.33 |
ribD | 2987249 | p.Glu137Asp | missense_variant | 0.17 |
Rv2752c | 3064527 | c.1665C>A | synonymous_variant | 0.21 |
Rv2752c | 3064565 | p.Glu543* | stop_gained | 0.2 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3064833 | c.1359C>A | synonymous_variant | 0.2 |
Rv2752c | 3065301 | c.891C>A | synonymous_variant | 0.2 |
Rv2752c | 3065388 | c.804C>A | synonymous_variant | 0.15 |
Rv2752c | 3065558 | p.Gly212Trp | missense_variant | 0.25 |
Rv2752c | 3065567 | p.Pro209Thr | missense_variant | 0.29 |
Rv2752c | 3065746 | p.Ser149Tyr | missense_variant | 0.29 |
Rv2752c | 3065800 | p.Gly131Asp | missense_variant | 1.0 |
Rv2752c | 3065957 | c.235T>C | synonymous_variant | 0.25 |
Rv2752c | 3066267 | c.-76C>A | upstream_gene_variant | 0.25 |
Rv2752c | 3066277 | c.-86C>A | upstream_gene_variant | 0.25 |
Rv2752c | 3067011 | c.-820C>A | upstream_gene_variant | 0.22 |
Rv2752c | 3067049 | c.-858G>T | upstream_gene_variant | 0.22 |
thyX | 3067222 | p.Ala242Ser | missense_variant | 0.15 |
thyX | 3067261 | p.Asp229Asn | missense_variant | 0.22 |
thyX | 3067357 | p.Ala197Ser | missense_variant | 0.18 |
thyX | 3067567 | p.Asp127Tyr | missense_variant | 0.25 |
thyX | 3067602 | p.Arg115Leu | missense_variant | 0.5 |
thyX | 3067613 | p.Glu111Asp | missense_variant | 0.33 |
thyX | 3067678 | p.Thr90Pro | missense_variant | 0.18 |
thyX | 3067720 | c.223_225delCAT | conservative_inframe_deletion | 0.33 |
thyX | 3067955 | c.-10G>T | upstream_gene_variant | 0.67 |
thyX | 3067978 | c.-33C>A | upstream_gene_variant | 0.4 |
thyX | 3067990 | c.-45C>A | upstream_gene_variant | 0.4 |
thyA | 3073869 | p.Trp201Cys | missense_variant | 0.33 |
thyA | 3073875 | p.Phe199Leu | missense_variant | 0.33 |
thyA | 3073887 | c.585G>T | synonymous_variant | 0.33 |
thyA | 3074025 | p.Phe149Leu | missense_variant | 0.25 |
thyA | 3074088 | c.384C>A | synonymous_variant | 0.29 |
thyA | 3074161 | p.Pro104Gln | missense_variant | 0.2 |
thyA | 3074555 | c.-84C>A | upstream_gene_variant | 0.23 |
thyA | 3074603 | c.-132G>T | upstream_gene_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087213 | p.Pro132Thr | missense_variant | 0.29 |
ald | 3087240 | p.Ala141Thr | missense_variant | 0.33 |
ald | 3087276 | p.Gln153Lys | missense_variant | 0.29 |
ald | 3087614 | c.795G>C | synonymous_variant | 0.12 |
ald | 3087676 | p.Pro286Gln | missense_variant | 0.18 |
ald | 3087686 | c.867C>A | synonymous_variant | 0.18 |
fbiD | 3338920 | c.-198G>T | upstream_gene_variant | 0.22 |
fbiD | 3339038 | c.-80C>A | upstream_gene_variant | 0.25 |
fbiD | 3339148 | p.Gly11Cys | missense_variant | 0.4 |
fbiD | 3339212 | p.Ala32Glu | missense_variant | 0.2 |
fbiD | 3339234 | c.117G>A | synonymous_variant | 0.25 |
fbiD | 3339250 | p.Asp45Tyr | missense_variant | 0.4 |
Rv3083 | 3448405 | c.-99G>T | upstream_gene_variant | 0.2 |
Rv3083 | 3448586 | p.Pro28His | missense_variant | 0.22 |
Rv3083 | 3448603 | p.Leu34Ile | missense_variant | 0.17 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448851 | p.Trp116Cys | missense_variant | 0.33 |
Rv3083 | 3448860 | c.357G>T | synonymous_variant | 0.22 |
Rv3083 | 3448888 | c.385C>A | synonymous_variant | 0.2 |
Rv3083 | 3448944 | c.441G>T | synonymous_variant | 0.18 |
Rv3083 | 3448956 | c.453G>T | synonymous_variant | 0.29 |
Rv3083 | 3449030 | p.Ser176Tyr | missense_variant | 0.5 |
Rv3083 | 3449258 | p.Arg252Leu | missense_variant | 0.33 |
Rv3083 | 3449346 | c.843G>T | synonymous_variant | 0.2 |
Rv3083 | 3449437 | p.Gly312Cys | missense_variant | 0.25 |
Rv3083 | 3449463 | p.Gln320His | missense_variant | 0.18 |
Rv3083 | 3449568 | c.1065G>T | synonymous_variant | 0.33 |
Rv3083 | 3449577 | c.1074C>A | synonymous_variant | 0.33 |
Rv3083 | 3449583 | c.1080G>T | synonymous_variant | 0.33 |
Rv3083 | 3449626 | p.Gly375Cys | missense_variant | 0.25 |
fprA | 3473998 | c.-9G>A | upstream_gene_variant | 1.0 |
fprA | 3473998 | c.-10_-9insA | upstream_gene_variant | 1.0 |
fprA | 3474075 | c.69G>T | synonymous_variant | 0.29 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474655 | p.Asp217Tyr | missense_variant | 0.25 |
fprA | 3474664 | p.Gly220Trp | missense_variant | 0.25 |
fprA | 3474756 | p.Lys250Asn | missense_variant | 0.17 |
fprA | 3474802 | p.Arg266Ser | missense_variant | 0.18 |
fprA | 3474957 | c.951G>T | synonymous_variant | 0.25 |
fprA | 3474961 | p.Val319Met | missense_variant | 1.0 |
fprA | 3475015 | p.Gln337Lys | missense_variant | 0.25 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fprA | 3475257 | c.1251G>T | synonymous_variant | 0.4 |
fprA | 3475298 | p.Arg431Leu | missense_variant | 0.4 |
whiB7 | 3568624 | p.Pro19Gln | missense_variant | 0.25 |
whiB7 | 3568648 | p.Pro11His | missense_variant | 0.22 |
whiB7 | 3568749 | c.-70A>T | upstream_gene_variant | 0.4 |
Rv3236c | 3611979 | p.Ala380Ser | missense_variant | 0.4 |
Rv3236c | 3612060 | p.Ala353Ser | missense_variant | 0.4 |
Rv3236c | 3612100 | c.1017C>A | synonymous_variant | 0.33 |
Rv3236c | 3612122 | p.Ala332Asp | missense_variant | 0.33 |
Rv3236c | 3612228 | c.889C>T | synonymous_variant | 0.33 |
Rv3236c | 3612266 | p.Pro284Gln | missense_variant | 0.67 |
Rv3236c | 3612334 | p.Met261Ile | missense_variant | 0.33 |
Rv3236c | 3612507 | p.His204Asn | missense_variant | 0.18 |
Rv3236c | 3612823 | c.294C>A | synonymous_variant | 0.33 |
Rv3236c | 3612999 | p.Gly40Cys | missense_variant | 0.25 |
Rv3236c | 3613054 | c.63G>T | synonymous_variant | 0.25 |
Rv3236c | 3613106 | p.Ser4* | stop_gained | 0.29 |
Rv3236c | 3613149 | c.-33G>T | upstream_gene_variant | 0.4 |
Rv3236c | 3613193 | c.-77C>A | upstream_gene_variant | 0.29 |
Rv3236c | 3613295 | c.-179G>T | upstream_gene_variant | 0.33 |
fbiA | 3640502 | c.-41C>A | upstream_gene_variant | 0.25 |
fbiA | 3640516 | c.-27G>T | upstream_gene_variant | 0.25 |
fbiA | 3640612 | p.Gly24Cys | missense_variant | 0.33 |
fbiA | 3640702 | p.His54Asn | missense_variant | 0.4 |
fbiA | 3640729 | p.Asp63His | missense_variant | 0.25 |
fbiA | 3640855 | p.Gly105Trp | missense_variant | 0.22 |
fbiB | 3640869 | c.-666G>T | upstream_gene_variant | 0.22 |
fbiA | 3640999 | p.His153Asn | missense_variant | 0.18 |
fbiB | 3641010 | c.-525C>A | upstream_gene_variant | 0.22 |
fbiA | 3641077 | p.Gln179Lys | missense_variant | 0.25 |
fbiA | 3641456 | p.Ser305* | stop_gained | 0.22 |
fbiB | 3641576 | c.42C>A | synonymous_variant | 0.29 |
fbiB | 3641813 | p.Leu93Phe | missense_variant | 0.2 |
fbiB | 3641883 | p.Glu117* | stop_gained | 0.2 |
fbiB | 3641915 | c.381C>A | synonymous_variant | 0.18 |
fbiB | 3642075 | p.Asp181Tyr | missense_variant | 0.5 |
fbiB | 3642207 | p.Asp225Tyr | missense_variant | 0.29 |
fbiB | 3642353 | c.819C>A | synonymous_variant | 0.18 |
fbiB | 3642575 | c.1041C>A | synonymous_variant | 0.29 |
fbiB | 3642758 | c.1224C>A | synonymous_variant | 0.29 |
alr | 3840213 | p.Arg403Leu | missense_variant | 0.2 |
alr | 3840489 | p.Pro311Gln | missense_variant | 0.29 |
alr | 3840574 | p.Leu283Met | missense_variant | 0.17 |
alr | 3840846 | p.Gly192Val | missense_variant | 0.17 |
alr | 3841131 | p.Ala97Glu | missense_variant | 0.29 |
alr | 3841145 | c.276C>A | synonymous_variant | 0.29 |
alr | 3841407 | p.Trp5Leu | missense_variant | 0.2 |
alr | 3841550 | c.-130G>T | upstream_gene_variant | 0.13 |
alr | 3841559 | c.-139C>A | upstream_gene_variant | 0.18 |
alr | 3841614 | c.-194C>A | upstream_gene_variant | 0.25 |
rpoA | 3877751 | p.Asp253Tyr | missense_variant | 0.2 |
rpoA | 3878105 | p.Glu135Lys | missense_variant | 0.18 |
rpoA | 3878130 | c.378C>A | synonymous_variant | 0.2 |
ddn | 3986700 | c.-144C>A | upstream_gene_variant | 0.29 |
ddn | 3987003 | p.Arg54Ser | missense_variant | 0.18 |
ddn | 3987042 | p.Leu67Met | missense_variant | 0.2 |
ddn | 3987289 | p.Cys149Tyr | missense_variant | 0.2 |
ddn | 3987296 | c.453C>A | synonymous_variant | 0.2 |
clpC1 | 4038390 | p.Pro772Gln | missense_variant | 0.25 |
clpC1 | 4038536 | c.2169C>A | synonymous_variant | 0.33 |
clpC1 | 4038571 | p.Arg712Ser | missense_variant | 0.29 |
clpC1 | 4038655 | p.Gly684Cys | missense_variant | 0.22 |
clpC1 | 4038818 | p.Lys629Asn | missense_variant | 0.17 |
clpC1 | 4039034 | c.1671C>A | synonymous_variant | 0.2 |
clpC1 | 4039058 | p.Phe549Leu | missense_variant | 0.33 |
clpC1 | 4039072 | p.Pro545Thr | missense_variant | 0.25 |
clpC1 | 4039154 | c.1551G>T | synonymous_variant | 0.22 |
clpC1 | 4039949 | c.756G>T | synonymous_variant | 0.18 |
clpC1 | 4040139 | p.Pro189Gln | missense_variant | 0.18 |
clpC1 | 4040208 | p.Ser166Tyr | missense_variant | 0.22 |
clpC1 | 4040214 | p.Ser164Tyr | missense_variant | 0.25 |
clpC1 | 4040229 | p.Gly159Val | missense_variant | 0.2 |
clpC1 | 4040240 | c.465C>A | synonymous_variant | 0.2 |
clpC1 | 4040306 | p.Arg133Ser | missense_variant | 0.18 |
clpC1 | 4040330 | c.375C>A | synonymous_variant | 0.2 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
panD | 4044118 | p.Leu55Pro | missense_variant | 0.33 |
panD | 4044288 | c.-7G>T | upstream_gene_variant | 0.4 |
panD | 4044412 | c.-131C>A | upstream_gene_variant | 0.2 |
embC | 4239881 | p.Pro7Thr | missense_variant | 0.25 |
embC | 4239928 | c.66G>T | synonymous_variant | 0.29 |
embC | 4240039 | p.Leu59Phe | missense_variant | 0.29 |
embC | 4240261 | c.399G>T | synonymous_variant | 0.33 |
embC | 4240279 | p.Leu139Phe | missense_variant | 0.33 |
embC | 4240459 | c.597G>T | synonymous_variant | 1.0 |
embC | 4240478 | p.Gly206Trp | missense_variant | 0.5 |
embC | 4240507 | c.645G>T | synonymous_variant | 0.4 |
embC | 4240572 | p.Gly237Val | missense_variant | 0.22 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240682 | p.Asp274Tyr | missense_variant | 0.2 |
embC | 4240737 | p.Ser292Tyr | missense_variant | 0.2 |
embC | 4240878 | p.Thr339Met | missense_variant | 0.33 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241081 | p.Leu407Met | missense_variant | 0.33 |
embC | 4241215 | c.1353C>A | synonymous_variant | 0.25 |
embC | 4241221 | c.1359C>A | synonymous_variant | 0.25 |
embC | 4241335 | p.Gln491His | missense_variant | 0.17 |
embC | 4241391 | p.Leu510Pro | missense_variant | 0.22 |
embC | 4241420 | p.Glu520* | stop_gained | 0.33 |
embC | 4241645 | p.Gly595Trp | missense_variant | 0.23 |
embC | 4241662 | c.1800G>T | synonymous_variant | 0.23 |
embC | 4241764 | p.Phe634Leu | missense_variant | 0.22 |
embA | 4242274 | c.-959G>T | upstream_gene_variant | 0.33 |
embC | 4242354 | p.Gly831Val | missense_variant | 0.4 |
embC | 4242459 | p.Ser866* | stop_gained | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242733 | p.Trp957Cys | missense_variant | 0.5 |
embA | 4243046 | c.-187C>A | upstream_gene_variant | 0.18 |
embA | 4243457 | c.225C>A | synonymous_variant | 0.29 |
embA | 4243505 | c.273C>A | synonymous_variant | 0.29 |
embA | 4243672 | p.Gly147Val | missense_variant | 0.29 |
embA | 4243679 | c.447C>A | synonymous_variant | 0.29 |
embA | 4243789 | p.Ser186* | stop_gained | 0.33 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244076 | c.844C>A | synonymous_variant | 0.2 |
embA | 4244167 | p.Ala312Val | missense_variant | 1.0 |
embA | 4244424 | p.Arg398Trp | missense_variant | 0.17 |
embA | 4244448 | c.1220delC | frameshift_variant | 0.15 |
embA | 4244615 | c.1383G>T | synonymous_variant | 0.5 |
embA | 4244921 | c.1689C>A | synonymous_variant | 0.2 |
embA | 4244955 | p.Gly575* | stop_gained | 0.25 |
embA | 4244984 | p.Leu584Phe | missense_variant | 0.25 |
embA | 4244993 | c.1761C>A | synonymous_variant | 0.38 |
embA | 4245079 | p.Trp616Leu | missense_variant | 0.2 |
embA | 4245089 | c.1857G>T | synonymous_variant | 0.18 |
embA | 4245125 | c.1893G>T | synonymous_variant | 0.29 |
embA | 4245149 | c.1917C>A | synonymous_variant | 0.33 |
embB | 4245617 | c.-897C>T | upstream_gene_variant | 0.25 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246081 | p.Pro950His | missense_variant | 0.18 |
embA | 4246094 | p.Phe954Leu | missense_variant | 0.22 |
embA | 4246182 | p.Ala984Thr | missense_variant | 0.4 |
embB | 4246244 | c.-270G>A | upstream_gene_variant | 0.22 |
embB | 4246248 | c.-266C>A | upstream_gene_variant | 0.22 |
embB | 4246259 | c.-255G>T | upstream_gene_variant | 0.22 |
embA | 4246413 | p.His1061Asn | missense_variant | 0.29 |
embB | 4246466 | c.-48G>T | upstream_gene_variant | 0.2 |
embB | 4246553 | p.Arg14Trp | missense_variant | 0.22 |
embB | 4246566 | p.Gly18Val | missense_variant | 0.25 |
embB | 4246642 | c.129G>T | synonymous_variant | 0.22 |
embB | 4246669 | c.156C>A | synonymous_variant | 0.18 |
embB | 4246721 | p.Pro70Thr | missense_variant | 0.29 |
embB | 4246744 | c.231C>A | synonymous_variant | 0.33 |
embB | 4246756 | c.243C>A | synonymous_variant | 0.33 |
embB | 4246787 | p.Pro92Thr | missense_variant | 0.25 |
embB | 4246814 | p.Thr101Ser | missense_variant | 0.33 |
embB | 4247073 | p.Gly187Val | missense_variant | 0.33 |
embB | 4247116 | c.603G>T | synonymous_variant | 0.33 |
embB | 4247135 | p.Thr208Ser | missense_variant | 0.33 |
embB | 4247138 | c.625C>A | synonymous_variant | 0.33 |
embB | 4247150 | c.637C>A | synonymous_variant | 0.33 |
embB | 4247183 | p.Gly224Trp | missense_variant | 0.29 |
embB | 4247376 | p.Leu288Pro | missense_variant | 0.15 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247667 | p.Trp385Leu | missense_variant | 0.29 |
embB | 4248709 | c.2196C>A | synonymous_variant | 0.29 |
embB | 4248887 | p.Gly792Arg | missense_variant | 0.18 |
embB | 4249438 | p.Gln975His | missense_variant | 0.22 |
embB | 4249561 | c.3048G>T | synonymous_variant | 0.18 |
embB | 4249604 | p.Gly1031Cys | missense_variant | 0.2 |
embB | 4249624 | c.3111C>A | synonymous_variant | 0.29 |
embB | 4249748 | p.Glu1079* | stop_gained | 0.4 |
embB | 4249753 | p.Leu1080Phe | missense_variant | 0.4 |
embB | 4249754 | p.Gly1081Cys | missense_variant | 0.4 |
embB | 4249797 | p.Arg1095Leu | missense_variant | 0.4 |
aftB | 4267397 | c.1440G>T | synonymous_variant | 0.25 |
aftB | 4267591 | p.Gln416Lys | missense_variant | 0.22 |
aftB | 4267636 | c.1201C>A | synonymous_variant | 0.18 |
aftB | 4267784 | c.1053G>T | synonymous_variant | 0.18 |
aftB | 4267811 | c.1026G>T | synonymous_variant | 0.29 |
aftB | 4267911 | p.Pro309Gln | missense_variant | 0.33 |
aftB | 4267948 | p.Asp297Tyr | missense_variant | 0.4 |
aftB | 4268344 | p.Arg165Ser | missense_variant | 0.38 |
aftB | 4268518 | p.Ala107Ser | missense_variant | 0.25 |
aftB | 4268535 | p.Gly101Val | missense_variant | 0.2 |
aftB | 4268552 | p.Met95Ile | missense_variant | 0.2 |
aftB | 4268561 | c.276G>T | synonymous_variant | 0.2 |
aftB | 4268565 | p.Ser91* | stop_gained | 0.2 |
aftB | 4268756 | c.81C>A | synonymous_variant | 0.29 |
aftB | 4268868 | c.-32G>T | upstream_gene_variant | 0.2 |
aftB | 4268872 | c.-36G>T | upstream_gene_variant | 0.2 |
aftB | 4268908 | c.-72C>A | upstream_gene_variant | 0.2 |
ubiA | 4268948 | p.Gly296Trp | missense_variant | 0.22 |
ubiA | 4269196 | p.Tyr213Phe | missense_variant | 0.15 |
aftB | 4269270 | c.-434G>T | upstream_gene_variant | 0.18 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269396 | c.-560G>T | upstream_gene_variant | 0.25 |
aftB | 4269489 | c.-653C>A | upstream_gene_variant | 0.2 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269727 | p.Pro36Leu | missense_variant | 0.29 |
ubiA | 4269788 | p.Gly16Trp | missense_variant | 0.22 |
aftB | 4269816 | c.-980G>A | upstream_gene_variant | 0.4 |
ubiA | 4269921 | c.-88C>A | upstream_gene_variant | 0.2 |
ubiA | 4269990 | c.-157G>T | upstream_gene_variant | 0.22 |
ethA | 4326046 | p.Glu476Asp | missense_variant | 0.17 |
ethA | 4326432 | p.Leu348Phe | missense_variant | 1.0 |
ethA | 4326535 | c.939G>T | synonymous_variant | 0.25 |
ethR | 4326820 | c.-729C>A | upstream_gene_variant | 0.18 |
ethA | 4327202 | p.Met91Thr | missense_variant | 0.11 |
ethA | 4327361 | p.Arg38Leu | missense_variant | 0.3 |
ethA | 4327528 | c.-55C>A | upstream_gene_variant | 0.4 |
ethR | 4327745 | p.Pro66Gln | missense_variant | 0.18 |
ethA | 4327788 | c.-315G>T | upstream_gene_variant | 0.36 |
ethR | 4327895 | p.Ser116* | stop_gained | 0.22 |
ethR | 4327931 | p.Arg128Met | missense_variant | 0.22 |
ethA | 4327956 | c.-483T>C | upstream_gene_variant | 0.18 |
ethA | 4328052 | c.-579G>T | upstream_gene_variant | 0.17 |
ethA | 4328273 | c.-800C>A | upstream_gene_variant | 0.2 |
ethA | 4328398 | c.-925C>A | upstream_gene_variant | 0.18 |
whiB6 | 4338193 | p.Arg110Leu | missense_variant | 0.2 |
whiB6 | 4338262 | p.Ala87Val | missense_variant | 0.33 |
whiB6 | 4338264 | c.258G>T | synonymous_variant | 0.33 |
whiB6 | 4338312 | c.210G>T | synonymous_variant | 0.18 |
whiB6 | 4338500 | p.Glu8* | stop_gained | 0.18 |
whiB6 | 4338535 | c.-14C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407542 | p.Gly221* | stop_gained | 0.17 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407643 | p.Arg187Met | missense_variant | 0.2 |
gid | 4407645 | c.558C>A | synonymous_variant | 0.18 |
gid | 4407660 | c.543G>T | synonymous_variant | 0.18 |
gid | 4407688 | p.Arg172Leu | missense_variant | 0.27 |
gid | 4407858 | c.345G>T | synonymous_variant | 0.25 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407878 | p.Gly109Cys | missense_variant | 0.33 |
gid | 4408324 | c.-122C>A | upstream_gene_variant | 0.18 |
gid | 4408445 | c.-243G>T | upstream_gene_variant | 0.25 |