Run ID: SRR6785268
Sample name:
Date: 04-04-2023 15:41:10
Number of reads: 2567898
Percentage reads mapped: 82.12
Strain: lineage4.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.95 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6238 | c.999G>A | synonymous_variant | 0.2 |
gyrB | 6242 | p.Arg335Asn | missense_variant | 0.2 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.19 |
gyrB | 6256 | c.1017G>A | synonymous_variant | 0.2 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.18 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.18 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.17 |
gyrB | 6289 | c.1050C>T | synonymous_variant | 0.17 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.17 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.18 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.18 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.13 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.15 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.15 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.15 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.16 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.17 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.17 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.13 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.14 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 0.13 |
fgd1 | 490917 | c.135C>G | synonymous_variant | 0.13 |
fgd1 | 491001 | c.219G>C | synonymous_variant | 0.15 |
fgd1 | 491007 | c.225G>C | synonymous_variant | 0.16 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.17 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.15 |
fgd1 | 491049 | c.267T>C | synonymous_variant | 0.14 |
fgd1 | 491247 | c.465C>T | synonymous_variant | 0.89 |
fgd1 | 491535 | c.753G>C | synonymous_variant | 0.16 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.17 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.16 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.15 |
fgd1 | 491553 | c.771G>A | synonymous_variant | 0.17 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.17 |
fgd1 | 491610 | c.828A>G | synonymous_variant | 0.18 |
fgd1 | 491616 | c.834A>G | synonymous_variant | 0.18 |
fgd1 | 491620 | p.Ile280Val | missense_variant | 0.17 |
fgd1 | 491643 | c.861G>A | synonymous_variant | 0.16 |
fgd1 | 491646 | c.864G>C | synonymous_variant | 0.17 |
fgd1 | 491649 | c.867C>T | synonymous_variant | 0.18 |
fgd1 | 491658 | c.876A>G | synonymous_variant | 0.17 |
fgd1 | 491661 | c.879C>G | synonymous_variant | 0.17 |
fgd1 | 491673 | c.891A>C | synonymous_variant | 0.17 |
fgd1 | 491676 | c.894T>C | synonymous_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.15 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.13 |
mshA | 575770 | c.423G>A | synonymous_variant | 0.16 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.16 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.21 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.2 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.15 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.17 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.17 |
mshA | 575830 | c.483C>G | synonymous_variant | 0.16 |
mshA | 575833 | c.486C>G | synonymous_variant | 0.14 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.14 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.18 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.18 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.18 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.17 |
mshA | 575908 | c.561A>G | synonymous_variant | 0.19 |
mshA | 575917 | p.Asp190Glu | missense_variant | 0.16 |
mshA | 575920 | c.573C>G | synonymous_variant | 0.16 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.2 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.14 |
ccsA | 620346 | c.456C>G | synonymous_variant | 0.19 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.17 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.19 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.19 |
ccsA | 620376 | c.486G>C | synonymous_variant | 0.18 |
ccsA | 620385 | c.495G>C | synonymous_variant | 0.18 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.17 |
ccsA | 620389 | c.499C>T | synonymous_variant | 0.17 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.17 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.16 |
ccsA | 620421 | c.531G>C | synonymous_variant | 0.13 |
ccsA | 620424 | c.534G>C | synonymous_variant | 0.18 |
ccsA | 620433 | c.543C>G | synonymous_variant | 0.17 |
ccsA | 620682 | c.792G>A | synonymous_variant | 0.14 |
ccsA | 620688 | c.798G>C | synonymous_variant | 0.14 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.21 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.19 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.19 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.19 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.19 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.2 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.21 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.15 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.14 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.15 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.15 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.13 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.17 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.16 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.15 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.16 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.14 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.15 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.15 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.15 |
rpoB | 760718 | c.912C>T | synonymous_variant | 0.14 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.14 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.13 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.15 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.14 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.14 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.2 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.14 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.14 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.15 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.17 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.13 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.14 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.17 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.18 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.17 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.15 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.16 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.15 |
rpoB | 761477 | c.1671C>G | synonymous_variant | 0.14 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.15 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.14 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.14 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.14 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.14 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.14 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.15 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.15 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.14 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.14 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.13 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.15 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.14 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.14 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.17 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.17 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.2 |
rpoC | 763025 | c.-345C>T | upstream_gene_variant | 0.2 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.21 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.22 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.2 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.21 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.19 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.19 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.14 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.14 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.14 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.16 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.18 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.18 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.18 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.19 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.19 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.21 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.21 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.21 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.16 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.15 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.19 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.17 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.24 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.23 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.21 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.22 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.2 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.2 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.2 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.18 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.17 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.17 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.2 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.19 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.17 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.14 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.14 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.13 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.15 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.15 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.15 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.19 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.19 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.18 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.19 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.19 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.16 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.15 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.15 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.16 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.16 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.14 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.13 |
rpoC | 764651 | p.Ser428Thr | missense_variant | 0.13 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.15 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.15 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.13 |
rpoC | 765327 | p.His653Pro | missense_variant | 0.13 |
rpoC | 765329 | p.Ser654Gly | missense_variant | 0.14 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.15 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.15 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.16 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.16 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.17 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.16 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.19 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.19 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.17 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.17 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.13 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.15 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.16 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.14 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.17 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.21 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.18 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.17 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.21 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.21 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 0.15 |
rpoC | 766885 | c.3516G>A | synonymous_variant | 0.15 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.15 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.15 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.15 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.18 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.15 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.17 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.13 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.14 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.15 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.14 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.17 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.15 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.17 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.14 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.13 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.16 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.16 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.13 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.14 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.14 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.14 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.14 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.14 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.15 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.17 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.15 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.15 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.14 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.14 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.15 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.15 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.17 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.14 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.14 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.14 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.15 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.18 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.16 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.15 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.16 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.16 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.14 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.14 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.14 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.14 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.16 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.19 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.21 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.21 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.19 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.18 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.19 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.2 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.22 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.22 |
fbiC | 1303944 | c.1014G>C | synonymous_variant | 0.17 |
fbiC | 1303947 | c.1017T>G | synonymous_variant | 0.16 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.16 |
fbiC | 1303953 | p.Asp341Glu | missense_variant | 0.16 |
fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.16 |
fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.16 |
fbiC | 1303971 | c.1041T>C | synonymous_variant | 0.16 |
fbiC | 1303980 | c.1050G>A | synonymous_variant | 0.2 |
fbiC | 1303998 | c.1068T>G | synonymous_variant | 0.21 |
fbiC | 1304004 | c.1074A>G | synonymous_variant | 0.21 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.21 |
fbiC | 1304022 | c.1092T>C | synonymous_variant | 0.16 |
fbiC | 1304031 | c.1101C>G | synonymous_variant | 0.18 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.18 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.17 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.17 |
fbiC | 1304049 | c.1119T>C | synonymous_variant | 0.17 |
fbiC | 1304050 | c.1120T>C | synonymous_variant | 0.17 |
fbiC | 1304058 | c.1128G>A | synonymous_variant | 0.14 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.14 |
fbiC | 1304064 | c.1134G>C | synonymous_variant | 0.14 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.15 |
fbiC | 1304085 | c.1155C>T | synonymous_variant | 0.16 |
fbiC | 1304091 | p.Asp387Glu | missense_variant | 0.14 |
fbiC | 1304092 | p.Met388Leu | missense_variant | 0.15 |
fbiC | 1304097 | c.1167G>C | synonymous_variant | 0.19 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.14 |
fbiC | 1304661 | c.1731C>T | synonymous_variant | 0.13 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.13 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475013 | n.1356G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.14 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.14 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.18 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.17 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.17 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.17 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.16 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.16 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.13 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.14 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.14 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.19 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.19 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.15 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.17 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.13 |
rpsA | 1834081 | c.540C>T | synonymous_variant | 0.17 |
rpsA | 1834105 | c.564C>G | synonymous_variant | 0.14 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.14 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 0.15 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.15 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.14 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.15 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.13 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918036 | p.Arg33Ser | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170266 | p.Gly116Asp | missense_variant | 1.0 |
PPE35 | 2170271 | c.342T>C | synonymous_variant | 1.0 |
PPE35 | 2170308 | p.Leu102Ala | missense_variant | 0.9 |
PPE35 | 2170313 | c.300G>C | synonymous_variant | 0.91 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.14 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.14 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.13 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.14 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.14 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.14 |
kasA | 2519137 | c.1023T>G | synonymous_variant | 0.14 |
kasA | 2519158 | c.1044C>T | synonymous_variant | 0.14 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.14 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.13 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.13 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.13 |
folC | 2746308 | p.Arg431Ser | missense_variant | 0.13 |
ribD | 2986910 | c.72C>A | synonymous_variant | 1.0 |
thyX | 3067284 | p.Ala221Gly | missense_variant | 0.13 |
thyX | 3067286 | c.660C>G | synonymous_variant | 0.13 |
thyX | 3067289 | c.657C>G | synonymous_variant | 0.13 |
thyX | 3067295 | c.651C>T | synonymous_variant | 0.13 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.15 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.17 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.16 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.18 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.16 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.16 |
thyX | 3067376 | c.570G>A | synonymous_variant | 0.17 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.22 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.22 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.32 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.34 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.38 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.41 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.38 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.42 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.44 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.33 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.29 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.3 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.27 |
thyX | 3067556 | p.His130Gln | missense_variant | 0.27 |
thyX | 3067559 | c.387C>G | synonymous_variant | 0.26 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.24 |
thyX | 3067570 | p.Ala126Pro | missense_variant | 0.2 |
thyX | 3067577 | c.369G>A | synonymous_variant | 0.21 |
thyX | 3067583 | c.363C>G | synonymous_variant | 0.19 |
thyX | 3067601 | p.Arg115His | missense_variant | 0.19 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.19 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.2 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.16 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.16 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.18 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.17 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.19 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.16 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.14 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.15 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.15 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.13 |
thyX | 3067772 | c.174C>G | synonymous_variant | 0.14 |
thyX | 3067781 | c.165C>A | synonymous_variant | 0.15 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.13 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.15 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.18 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.17 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.17 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.17 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.17 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.16 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.17 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.15 |
thyX | 3067898 | p.Asp16Glu | missense_variant | 0.15 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.14 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 0.91 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.14 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.13 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.14 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.13 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.15 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.15 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.15 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.13 |
rpoA | 3878043 | c.465G>A | synonymous_variant | 0.13 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.13 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.14 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.15 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.16 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.16 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242754 | c.-479G>C | upstream_gene_variant | 0.13 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.13 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.14 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.15 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.17 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.17 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.15 |
embB | 4249594 | c.3081G>A | synonymous_variant | 0.97 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 0.96 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
PPE35 | 2167033 | c.346_*615del | stop_lost&conservative_inframe_deletion&splice_region_variant | 1.0 |