Run ID: SRR1173113
Sample name:
Date: 03-04-2023 03:16:48
Number of reads: 186960
Percentage reads mapped: 1.77
Strain: lineage4.3.4
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.06 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761095 | p.Leu430Pro | missense_variant | 1.0 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.99 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6123 | p.Ala295Asp | missense_variant | 0.67 |
gyrB | 6521 | p.Arg428Trp | missense_variant | 0.67 |
gyrA | 7198 | c.-104C>A | upstream_gene_variant | 0.25 |
gyrB | 7215 | p.Arg659Gln | missense_variant | 0.5 |
gyrA | 7274 | c.-28C>A | upstream_gene_variant | 1.0 |
gyrA | 7342 | p.Arg14Gln | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9113 | c.1812C>A | synonymous_variant | 0.67 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490623 | c.-160G>T | upstream_gene_variant | 0.67 |
fgd1 | 491288 | p.Gly169Asp | missense_variant | 1.0 |
mshA | 575543 | p.Gly66Ser | missense_variant | 0.67 |
mshA | 576223 | c.876G>T | synonymous_variant | 0.5 |
mshA | 576244 | c.897C>A | synonymous_variant | 0.5 |
rpoB | 759837 | p.Ala11Thr | missense_variant | 0.67 |
rpoB | 759868 | p.Ser21Tyr | missense_variant | 0.5 |
rpoB | 760232 | p.Lys142Asn | missense_variant | 0.29 |
rpoB | 760251 | p.Gly149Cys | missense_variant | 0.33 |
rpoB | 760292 | c.486C>A | synonymous_variant | 0.25 |
rpoB | 761458 | p.Pro551Gln | missense_variant | 0.4 |
rpoB | 761655 | p.Ala617Ser | missense_variant | 0.5 |
rpoC | 762812 | c.-558C>A | upstream_gene_variant | 0.67 |
rpoC | 763405 | c.36C>T | synonymous_variant | 0.33 |
rpoC | 765082 | c.1713G>T | synonymous_variant | 0.67 |
rpoC | 765099 | p.Pro577Leu | missense_variant | 0.67 |
rpoC | 765448 | p.Gln693His | missense_variant | 0.5 |
mmpL5 | 776148 | p.Ile778Thr | missense_variant | 0.22 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.22 |
mmpL5 | 776483 | p.Met666Ile | missense_variant | 0.33 |
mmpL5 | 777856 | p.Ala209Ser | missense_variant | 0.4 |
mmpS5 | 779534 | c.-629C>A | upstream_gene_variant | 0.5 |
rplC | 801181 | p.Gly125Ser | missense_variant | 1.0 |
fbiC | 1302825 | c.-106C>A | upstream_gene_variant | 0.67 |
fbiC | 1303226 | p.Arg99Leu | missense_variant | 0.5 |
fbiC | 1303720 | p.Gly264Cys | missense_variant | 0.5 |
fbiC | 1304013 | c.1083G>A | synonymous_variant | 0.5 |
fbiC | 1304028 | p.Asn366Lys | missense_variant | 0.33 |
embR | 1417007 | p.Arg114Gln | missense_variant | 0.67 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471873 | n.28C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.99 |
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 | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.96 |
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 | 0.99 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473316 | n.1471C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473318 | n.1473G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1473869 | n.212C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474233 | n.576C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474848 | n.1191G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474862 | n.1205C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475359 | n.1702G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475361 | n.1704G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475634 | n.1977G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476117 | n.2460G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476126 | n.2469C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476135 | n.2478T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.29 |
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 | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.99 |
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 | 0.98 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673361 | c.-79C>A | upstream_gene_variant | 0.5 |
fabG1 | 1673471 | p.Pro11His | missense_variant | 0.29 |
inhA | 1674213 | c.12G>A | synonymous_variant | 0.67 |
rpsA | 1833937 | p.Glu132Asp | missense_variant | 1.0 |
rpsA | 1834943 | p.Ala468Pro | missense_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918110 | p.Asp57Glu | missense_variant | 0.5 |
ndh | 2101697 | p.Ala449Asp | missense_variant | 1.0 |
ndh | 2102827 | c.216C>T | synonymous_variant | 0.67 |
katG | 2154522 | p.Ser530* | stop_gained | 0.5 |
PPE35 | 2167746 | p.Thr956Asn | missense_variant | 0.29 |
PPE35 | 2167985 | p.Met876Ile | missense_variant | 1.0 |
PPE35 | 2167997 | c.2616G>T | synonymous_variant | 0.67 |
PPE35 | 2168408 | c.2205C>A | synonymous_variant | 0.33 |
PPE35 | 2168894 | c.1719C>A | synonymous_variant | 0.29 |
PPE35 | 2169416 | c.1197G>T | synonymous_variant | 0.67 |
PPE35 | 2169445 | p.Gly390Cys | missense_variant | 0.5 |
PPE35 | 2169460 | p.Gly385Cys | missense_variant | 0.5 |
PPE35 | 2169551 | c.1062C>A | synonymous_variant | 0.29 |
PPE35 | 2169604 | p.Gly337Cys | missense_variant | 0.29 |
PPE35 | 2170268 | c.345C>T | synonymous_variant | 0.67 |
PPE35 | 2170731 | c.-119C>A | upstream_gene_variant | 0.5 |
Rv1979c | 2221734 | c.1431G>T | synonymous_variant | 0.5 |
Rv1979c | 2222638 | p.Ala176Glu | missense_variant | 0.5 |
Rv1979c | 2223059 | p.Pro36Thr | missense_variant | 0.4 |
Rv1979c | 2223099 | c.66C>T | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>T | upstream_gene_variant | 1.0 |
kasA | 2518298 | p.Gly62Cys | missense_variant | 1.0 |
ahpC | 2726597 | c.405C>A | synonymous_variant | 0.5 |
folC | 2746216 | p.Phe461Leu | missense_variant | 1.0 |
folC | 2746707 | p.Gln298* | stop_gained | 0.67 |
folC | 2746780 | c.819C>T | synonymous_variant | 0.4 |
folC | 2747658 | c.-60C>A | upstream_gene_variant | 0.5 |
ribD | 2986923 | p.Pro29Ser | missense_variant | 0.29 |
ribD | 2987017 | p.Gly60Val | missense_variant | 0.67 |
Rv2752c | 3065318 | p.Ala292Thr | missense_variant | 0.5 |
Rv2752c | 3065324 | p.Ala290Ser | missense_variant | 0.5 |
Rv2752c | 3065325 | c.867C>T | synonymous_variant | 0.5 |
Rv2752c | 3065631 | c.561C>T | synonymous_variant | 1.0 |
Rv2752c | 3065878 | p.Ser105* | stop_gained | 0.67 |
thyX | 3067773 | p.Ala58Asp | missense_variant | 0.5 |
thyA | 3074124 | c.348G>A | synonymous_variant | 1.0 |
thyA | 3074666 | c.-195G>T | upstream_gene_variant | 0.25 |
ald | 3086667 | c.-153C>G | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087144 | p.Asp109Tyr | missense_variant | 1.0 |
Rv3083 | 3449044 | p.Val181Ile | missense_variant | 0.67 |
fprA | 3474803 | p.Arg266Leu | missense_variant | 1.0 |
whiB7 | 3568670 | p.Leu4Met | missense_variant | 1.0 |
Rv3236c | 3613105 | c.12G>T | synonymous_variant | 0.5 |
fbiB | 3642709 | p.Gly392Val | missense_variant | 0.5 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
alr | 3841390 | p.Pro11Thr | missense_variant | 0.25 |
rpoA | 3878169 | c.339G>T | synonymous_variant | 0.5 |
rpoA | 3878336 | p.Gly58Cys | missense_variant | 0.5 |
clpC1 | 4039221 | p.Pro495Leu | missense_variant | 1.0 |
clpC1 | 4039811 | c.894C>T | synonymous_variant | 0.33 |
clpC1 | 4040476 | p.His77Tyr | missense_variant | 0.4 |
embC | 4241116 | c.1254C>A | synonymous_variant | 0.33 |
embC | 4241952 | p.Arg697Met | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243517 | c.285C>T | synonymous_variant | 1.0 |
embA | 4246306 | p.Ser1025* | stop_gained | 1.0 |
embB | 4247932 | c.1419C>T | synonymous_variant | 1.0 |
embB | 4248239 | p.Gly576Cys | missense_variant | 0.33 |
aftB | 4267122 | p.Arg572Leu | missense_variant | 0.33 |
aftB | 4268112 | p.Ala242Val | missense_variant | 0.67 |
aftB | 4268402 | p.Leu145Phe | missense_variant | 1.0 |
ubiA | 4269722 | p.Ala38Thr | missense_variant | 1.0 |
ethA | 4326069 | p.Arg469Trp | missense_variant | 0.4 |
ethA | 4326759 | p.Arg239Trp | missense_variant | 0.29 |
ethA | 4327257 | p.Gln73Lys | missense_variant | 0.5 |
ethA | 4327502 | c.-29C>A | upstream_gene_variant | 0.5 |
ethA | 4328013 | c.-540G>A | upstream_gene_variant | 0.4 |
ethA | 4328222 | c.-749G>T | upstream_gene_variant | 1.0 |
whiB6 | 4338257 | p.Ala89Ser | missense_variant | 1.0 |
whiB6 | 4338313 | p.Ala70Glu | missense_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407852 | c.351G>T | synonymous_variant | 0.67 |