Run ID: SRR3105762
Sample name:
Date: 04-04-2023 05:08:15
Number of reads: 304302
Percentage reads mapped: 7.59
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.83 | isoniazid |
pncA | 2288764 | p.Thr160Pro | missense_variant | 0.4 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.29 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.5 |
rpoB | 761850 | p.Pro682Ala | missense_variant | 0.7 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.5 |
rpoB | 762911 | p.Ile1035Met | missense_variant | 0.4 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.6 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.6 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.6 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.78 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.7 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.64 |
rpoC | 762965 | c.-405T>C | upstream_gene_variant | 0.64 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.5 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 0.33 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.5 |
rpoC | 764263 | c.894G>A | synonymous_variant | 0.67 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.95 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.96 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.96 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.95 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.92 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.9 |
rpoC | 764731 | c.1362G>T | synonymous_variant | 0.8 |
rpoC | 764735 | p.Val456Met | missense_variant | 0.67 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.33 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 0.6 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407537 | c.-197G>T | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472108 | n.263C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472135 | n.290C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472139 | n.294C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472243 | n.398G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472253 | n.408G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472279 | n.434T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472333 | n.488G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472956 | n.1111T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473054 | n.1209C>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473070 | n.1225G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473071 | n.1226C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473147 | n.1302G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473204 | n.1359C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475632 | n.1975C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476528 | n.2871A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476535 | n.2878G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476545 | n.2888C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476565 | n.2908G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.62 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
thyX | 3067452 | p.Lys165Thr | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
ddn | 3987259 | p.Trp139* | stop_gained | 0.6 |
clpC1 | 4039522 | c.1183C>T | synonymous_variant | 0.33 |
clpC1 | 4039528 | c.1177C>A | synonymous_variant | 0.5 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.5 |
clpC1 | 4039544 | c.1161C>T | synonymous_variant | 0.67 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.33 |
clpC1 | 4039674 | p.Pro344Lys | missense_variant | 0.29 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.55 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.43 |
clpC1 | 4040032 | p.Val225Ile | missense_variant | 0.5 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.5 |
clpC1 | 4040036 | c.669C>T | synonymous_variant | 0.5 |
clpC1 | 4040045 | c.660C>G | synonymous_variant | 0.5 |
clpC1 | 4040054 | c.651G>A | synonymous_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249757 | p.Thr1082Ala | missense_variant | 0.67 |
ubiA | 4269307 | p.Phe176Ser | missense_variant | 0.8 |
ethA | 4326197 | p.Val426Gly | missense_variant | 0.8 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.6 |