Run ID: SRR1173521
Sample name:
Date: 03-04-2023 03:26:37
Number of reads: 182555
Percentage reads mapped: 1.76
Strain: lineage4.9
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.94 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.98 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.75 | isoniazid |
katG | 2155192 | p.Gly307Glu | missense_variant | 0.5 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrB | 6524 | p.Arg429Ser | missense_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8544 | p.Asp415Tyr | missense_variant | 0.5 |
gyrA | 8597 | c.1296C>A | synonymous_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490861 | p.Ala27Ser | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.5 |
mshA | 576128 | p.Leu261Ile | missense_variant | 0.67 |
ccsA | 619694 | c.-197C>A | upstream_gene_variant | 1.0 |
ccsA | 620402 | p.Trp171Leu | missense_variant | 1.0 |
ccsA | 620499 | c.609G>T | synonymous_variant | 0.67 |
ccsA | 620544 | c.654G>T | synonymous_variant | 1.0 |
rpoB | 761752 | p.Ala649Asp | missense_variant | 0.4 |
rpoB | 762522 | p.Pro906Thr | missense_variant | 0.33 |
rpoB | 762774 | p.Arg990Ser | missense_variant | 0.5 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766219 | p.Asp950Glu | missense_variant | 0.29 |
rpoC | 766223 | c.2854C>T | synonymous_variant | 0.29 |
rpoC | 766230 | p.Ala954Asp | missense_variant | 0.29 |
rpoC | 767092 | c.3723C>T | synonymous_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776766 | p.Ala572Val | missense_variant | 0.29 |
mmpL5 | 777635 | c.846C>A | synonymous_variant | 0.4 |
mmpL5 | 778992 | c.-512C>A | upstream_gene_variant | 0.2 |
mmpR5 | 779006 | p.Gly6Val | missense_variant | 0.22 |
mmpR5 | 779186 | p.Gly66Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801330 | c.522G>T | synonymous_variant | 0.67 |
fbiC | 1302975 | c.45C>A | synonymous_variant | 1.0 |
fbiC | 1303001 | p.Ser24* | stop_gained | 1.0 |
fbiC | 1304866 | p.Gly646Trp | missense_variant | 1.0 |
fbiC | 1304878 | p.Arg650Cys | missense_variant | 1.0 |
fbiC | 1304910 | c.1980G>T | synonymous_variant | 0.5 |
embR | 1417373 | c.-26G>A | upstream_gene_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473287 | n.1442C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474128 | n.471G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474198 | n.541G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474848 | n.1191G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474862 | n.1205C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475534 | n.1877G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475613 | n.1956A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475961 | n.2304C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476131 | n.2474C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476565 | n.2908G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476568 | n.2911G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476599 | n.2942C>T | non_coding_transcript_exon_variant | 0.67 |
inhA | 1673366 | c.-836G>A | upstream_gene_variant | 0.5 |
fabG1 | 1673891 | p.Ala151Asp | missense_variant | 0.33 |
inhA | 1674953 | p.Pro251Leu | missense_variant | 0.67 |
rpsA | 1834856 | p.Glu439Lys | missense_variant | 0.5 |
tlyA | 1917904 | c.-36C>T | upstream_gene_variant | 0.4 |
ndh | 2102438 | p.Arg202Leu | missense_variant | 1.0 |
katG | 2154077 | p.Gln679* | stop_gained | 0.5 |
katG | 2154588 | c.1524C>T | synonymous_variant | 1.0 |
katG | 2154996 | c.1116G>T | synonymous_variant | 1.0 |
katG | 2156268 | c.-157G>T | upstream_gene_variant | 0.5 |
PPE35 | 2168736 | p.Ser626Ile | missense_variant | 0.4 |
PPE35 | 2169101 | c.1512G>A | synonymous_variant | 0.5 |
PPE35 | 2169677 | c.936C>A | synonymous_variant | 0.18 |
PPE35 | 2169852 | p.Gly254Val | missense_variant | 0.4 |
Rv1979c | 2221731 | c.1434G>A | synonymous_variant | 0.33 |
Rv1979c | 2221778 | p.Ala463Ser | missense_variant | 0.22 |
Rv1979c | 2221843 | p.Arg441Leu | missense_variant | 0.33 |
Rv1979c | 2221940 | c.1225C>A | synonymous_variant | 1.0 |
Rv1979c | 2222036 | p.Leu377Met | missense_variant | 0.4 |
Rv1979c | 2222082 | c.1083C>A | synonymous_variant | 0.22 |
Rv1979c | 2222313 | c.852G>A | synonymous_variant | 0.25 |
Rv1979c | 2223253 | c.-89C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223305 | c.-141G>T | upstream_gene_variant | 0.4 |
pncA | 2288804 | c.438G>T | synonymous_variant | 1.0 |
pncA | 2289995 | c.-754C>A | upstream_gene_variant | 0.67 |
pncA | 2290048 | c.-807C>A | upstream_gene_variant | 0.67 |
kasA | 2519218 | c.1104G>T | synonymous_variant | 0.5 |
folC | 2746482 | c.1117C>A | synonymous_variant | 1.0 |
folC | 2746647 | p.Gln318Lys | missense_variant | 0.67 |
pepQ | 2859524 | p.Gly299Cys | missense_variant | 0.29 |
pepQ | 2860306 | p.Gly38Val | missense_variant | 0.5 |
thyA | 3073758 | p.Ile238Met | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086879 | c.60G>A | synonymous_variant | 0.67 |
ald | 3087356 | c.537C>T | synonymous_variant | 0.5 |
ald | 3087598 | p.Pro260Gln | missense_variant | 1.0 |
fprA | 3473955 | c.-52G>T | upstream_gene_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612635 | p.Ala161Glu | missense_variant | 0.4 |
fbiB | 3642382 | p.Ala283Asp | missense_variant | 1.0 |
rpoA | 3878043 | c.465G>T | synonymous_variant | 0.33 |
rpoA | 3878276 | p.Leu78Met | missense_variant | 0.67 |
ddn | 3986841 | c.-3G>T | upstream_gene_variant | 0.4 |
ddn | 3987084 | p.Gly81Cys | missense_variant | 0.5 |
panD | 4044113 | c.168delC | frameshift_variant | 0.25 |
panD | 4044216 | p.Tyr22* | stop_gained | 0.4 |
panD | 4044377 | c.-96G>T | upstream_gene_variant | 0.67 |
panD | 4044397 | c.-116G>T | upstream_gene_variant | 0.5 |
panD | 4044438 | c.-157G>T | upstream_gene_variant | 0.5 |
embC | 4240446 | p.Pro195Gln | missense_variant | 0.67 |
embC | 4242233 | p.Pro791Ser | missense_variant | 1.0 |
embC | 4242273 | p.Gly804Val | missense_variant | 0.5 |
embC | 4242633 | p.Pro924Leu | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242776 | p.Gln972Lys | missense_variant | 0.67 |
embA | 4244076 | c.844C>A | synonymous_variant | 1.0 |
embA | 4244384 | c.1152G>T | synonymous_variant | 0.33 |
embB | 4249183 | c.2670C>T | synonymous_variant | 0.67 |
embB | 4249375 | c.2862G>T | synonymous_variant | 1.0 |
embB | 4249496 | p.Pro995Thr | missense_variant | 1.0 |
aftB | 4267701 | p.Trp379Leu | missense_variant | 1.0 |
aftB | 4267729 | p.Trp370Arg | missense_variant | 1.0 |
aftB | 4267731 | p.Arg369Leu | missense_variant | 1.0 |
aftB | 4267880 | c.957C>A | synonymous_variant | 1.0 |
aftB | 4268096 | c.741C>A | synonymous_variant | 0.4 |
aftB | 4268137 | p.Leu234Met | missense_variant | 0.4 |
ubiA | 4269722 | p.Ala38Thr | missense_variant | 0.67 |
ethA | 4326758 | p.Arg239Gln | missense_variant | 1.0 |
ethR | 4327321 | c.-228G>A | upstream_gene_variant | 0.67 |
ethA | 4327830 | c.-357G>T | upstream_gene_variant | 0.5 |
ethA | 4328222 | c.-749G>A | upstream_gene_variant | 0.67 |
whiB6 | 4338243 | c.279C>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |