Run ID: SRR1175304
Sample name:
Date: 03-04-2023 03:38:49
Number of reads: 795680
Percentage reads mapped: 12.1
Strain: lineage4.3.3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761161 | p.Leu452Pro | missense_variant | 0.89 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.92 | streptomycin |
fabG1 | 1673432 | c.-8T>A | upstream_gene_variant | 1.0 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288785 | c.456dupC | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4327484 | c.-11A>G | upstream_gene_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8457 | p.Glu386* | stop_gained | 0.14 |
gyrA | 8918 | c.1617C>A | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490926 | c.144C>T | synonymous_variant | 0.22 |
mshA | 575914 | c.567C>T | synonymous_variant | 0.29 |
mshA | 575959 | p.Gln204His | missense_variant | 0.2 |
mshA | 576461 | p.Ala372Thr | missense_variant | 0.33 |
ccsA | 619740 | c.-151C>T | upstream_gene_variant | 0.25 |
ccsA | 620554 | p.Ala222Ser | missense_variant | 0.15 |
rpoB | 760334 | c.528G>T | synonymous_variant | 0.13 |
rpoB | 760658 | p.Glu284Asp | missense_variant | 0.22 |
rpoB | 761239 | p.Cys478Phe | missense_variant | 0.18 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.13 |
rpoB | 763086 | p.Val1094Phe | missense_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.95 |
rpoC | 765862 | p.Phe831Leu | missense_variant | 0.13 |
rpoC | 765890 | p.Arg841Gly | missense_variant | 0.11 |
rpoC | 766014 | c.2647delG | frameshift_variant | 0.22 |
rpoC | 766490 | p.Arg1041Ser | missense_variant | 0.14 |
rpoC | 766594 | c.3225G>T | synonymous_variant | 0.25 |
rpoC | 766714 | c.3345G>T | synonymous_variant | 0.29 |
rpoC | 767108 | p.Gly1247Cys | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777035 | p.Gln482His | missense_variant | 0.18 |
mmpR5 | 779254 | p.Arg89Trp | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781657 | p.Val33Glu | missense_variant | 0.12 |
rplC | 800867 | p.Ser20Ile | missense_variant | 0.15 |
rplC | 801049 | p.Leu81Met | missense_variant | 0.14 |
fbiC | 1303120 | p.Arg64Trp | missense_variant | 0.29 |
fbiC | 1303872 | p.Tyr314* | stop_gained | 0.22 |
fbiC | 1304323 | p.Asp465Tyr | missense_variant | 0.17 |
fbiC | 1304611 | p.Gly561Ser | missense_variant | 0.2 |
fbiC | 1305442 | p.Glu838Lys | missense_variant | 0.15 |
Rv1258c | 1406716 | p.Val209Leu | missense_variant | 0.12 |
Rv1258c | 1406732 | c.609G>T | synonymous_variant | 0.12 |
Rv1258c | 1406988 | p.Pro118Gln | missense_variant | 0.22 |
Rv1258c | 1407416 | c.-76C>A | upstream_gene_variant | 0.18 |
embR | 1416621 | p.Pro243Thr | missense_variant | 0.17 |
embR | 1417138 | c.210G>T | synonymous_variant | 0.18 |
atpE | 1461095 | p.Met17Ile | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474516 | n.859C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474674 | n.1018delC | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474709 | n.1052G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474848 | n.1191G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474862 | n.1205C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1833876 | p.Ala112Asp | missense_variant | 0.22 |
rpsA | 1833914 | p.Ala125Ser | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918650 | c.711C>T | synonymous_variant | 0.14 |
ndh | 2102827 | c.216C>A | synonymous_variant | 0.14 |
katG | 2154168 | p.Glu648Asp | missense_variant | 0.22 |
katG | 2155506 | c.606C>A | synonymous_variant | 0.18 |
katG | 2156042 | p.Gly24Cys | missense_variant | 0.22 |
PPE35 | 2167909 | p.Gly902* | stop_gained | 0.14 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.19 |
PPE35 | 2170290 | p.Ala108Glu | missense_variant | 0.17 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 0.89 |
Rv1979c | 2223078 | c.87C>T | synonymous_variant | 0.22 |
Rv1979c | 2223156 | c.9C>A | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518623 | p.Ala170Asp | missense_variant | 0.2 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2714477 | p.Arg286Ser | missense_variant | 0.15 |
eis | 2714712 | c.621G>T | synonymous_variant | 0.12 |
eis | 2714937 | c.396G>T | synonymous_variant | 0.12 |
eis | 2715000 | c.333C>A | synonymous_variant | 0.17 |
eis | 2715206 | p.Asp43Asn | missense_variant | 0.15 |
eis | 2715441 | c.-109C>T | upstream_gene_variant | 0.12 |
folC | 2746903 | c.696G>T | synonymous_variant | 0.18 |
folC | 2747001 | p.Asp200Tyr | missense_variant | 0.17 |
pepQ | 2859603 | c.816G>T | synonymous_variant | 0.14 |
pepQ | 2860247 | p.Gly58Cys | missense_variant | 0.2 |
Rv2752c | 3064809 | c.1383C>T | synonymous_variant | 0.25 |
Rv2752c | 3065385 | p.Asn269Lys | missense_variant | 0.12 |
Rv2752c | 3065657 | p.Asp179His | missense_variant | 0.15 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087201 | p.Pro128Ser | missense_variant | 0.2 |
ald | 3087271 | p.Arg151Gln | missense_variant | 0.2 |
ald | 3087441 | p.Asp208Tyr | missense_variant | 0.14 |
ald | 3087471 | p.Arg218Cys | missense_variant | 0.18 |
ald | 3087749 | c.930C>A | synonymous_variant | 0.17 |
ald | 3087813 | p.Ala332Ser | missense_variant | 0.15 |
fbiD | 3339556 | p.Gly147Cys | missense_variant | 0.13 |
Rv3083 | 3448616 | p.Arg38Pro | missense_variant | 0.1 |
Rv3083 | 3449339 | p.Arg279His | missense_variant | 0.15 |
Rv3083 | 3449856 | p.Met451Ile | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474228 | c.222C>A | synonymous_variant | 0.12 |
fprA | 3475285 | p.Asp427Asn | missense_variant | 0.18 |
Rv3236c | 3612178 | c.939C>A | synonymous_variant | 0.12 |
Rv3236c | 3612454 | c.663G>A | synonymous_variant | 0.12 |
Rv3236c | 3613249 | c.-135_-134delCG | upstream_gene_variant | 0.17 |
fbiB | 3642711 | p.Leu393Val | missense_variant | 0.14 |
rpoA | 3877531 | p.Ala326Asp | missense_variant | 0.14 |
rpoA | 3878386 | p.Thr41Asn | missense_variant | 0.2 |
ddn | 3986725 | c.-119G>T | upstream_gene_variant | 0.18 |
ddn | 3986745 | c.-99A>G | upstream_gene_variant | 0.14 |
ddn | 3987074 | c.231C>A | synonymous_variant | 0.12 |
clpC1 | 4038203 | p.Lys834Asn | missense_variant | 0.14 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038389 | c.2316G>A | synonymous_variant | 0.22 |
clpC1 | 4038428 | c.2277G>T | synonymous_variant | 0.18 |
clpC1 | 4039013 | c.1692G>A | synonymous_variant | 0.17 |
clpC1 | 4039141 | c.1563delA | frameshift_variant | 0.17 |
clpC1 | 4039474 | p.Arg411Trp | missense_variant | 0.17 |
clpC1 | 4039886 | c.819C>A | synonymous_variant | 0.13 |
clpC1 | 4040856 | c.-152G>T | upstream_gene_variant | 0.14 |
panD | 4044009 | c.273G>T | synonymous_variant | 0.12 |
embC | 4239846 | c.-17C>T | upstream_gene_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243383 | p.Ala51Ser | missense_variant | 0.17 |
embA | 4243782 | p.Gly184Trp | missense_variant | 0.18 |
embA | 4243791 | p.Ala187Ser | missense_variant | 0.18 |
embA | 4243908 | p.Arg226Trp | missense_variant | 0.18 |
embA | 4244770 | p.Gly513Val | missense_variant | 0.2 |
embA | 4244878 | p.Ala549Asp | missense_variant | 0.29 |
embA | 4245195 | p.Ile655Phe | missense_variant | 0.13 |
embB | 4246256 | c.-258G>T | upstream_gene_variant | 0.22 |
embB | 4246566 | p.Gly18Val | missense_variant | 0.25 |
embB | 4246976 | p.Ala155Ser | missense_variant | 0.12 |
embB | 4247203 | c.690C>A | synonymous_variant | 0.33 |
embB | 4248128 | p.Arg539Trp | missense_variant | 0.14 |
embB | 4248155 | p.Leu548Ile | missense_variant | 0.14 |
embB | 4248855 | p.Gly781Asp | missense_variant | 0.18 |
embB | 4249374 | p.Ser954Trp | missense_variant | 0.11 |
aftB | 4268662 | p.Thr59Ala | missense_variant | 0.15 |
aftB | 4268811 | p.Ser9Leu | missense_variant | 0.22 |
ubiA | 4269271 | p.Val188Ala | missense_variant | 1.0 |
ubiA | 4269684 | p.Glu50Asp | missense_variant | 0.22 |
ubiA | 4269983 | c.-150C>T | upstream_gene_variant | 0.22 |
ethA | 4326762 | p.Val238Leu | missense_variant | 0.13 |
ethA | 4327328 | p.Arg49His | missense_variant | 0.18 |
ethA | 4327425 | p.Val17Ile | missense_variant | 0.12 |
ethR | 4327964 | p.Ser139* | stop_gained | 0.2 |
ethR | 4328185 | p.Gly213Cys | missense_variant | 0.15 |
ethA | 4328312 | c.-839C>T | upstream_gene_variant | 0.15 |
ethA | 4328398 | c.-925C>T | upstream_gene_variant | 0.22 |
whiB6 | 4338215 | p.Gly103Cys | missense_variant | 0.33 |
whiB6 | 4338321 | c.201C>A | synonymous_variant | 0.17 |
whiB6 | 4338361 | p.Arg54Leu | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407563 | p.Gly214Trp | missense_variant | 0.22 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408185 | c.18C>A | synonymous_variant | 0.18 |
gid | 4407912 | c.160_290del | frameshift_variant | 1.0 |