Run ID: SRR1140627
Sample name:
Date: 02-04-2023 20:56:58
Number of reads: 623418
Percentage reads mapped: 19.81
Strain: lineage4.6.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918634 | p.Gly232Asp | missense_variant | 0.13 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5188 | c.-52C>A | upstream_gene_variant | 0.12 |
gyrB | 5537 | p.Met100Leu | missense_variant | 0.13 |
gyrB | 6020 | p.Val261Met | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7539 | p.Thr80Ala | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7629 | p.Val110Met | missense_variant | 0.18 |
gyrA | 7881 | p.Leu194Met | missense_variant | 0.18 |
gyrA | 8621 | p.Leu440Phe | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9435 | p.Leu712Met | missense_variant | 0.14 |
fgd1 | 491321 | p.Ala180Val | missense_variant | 0.25 |
mshA | 575242 | c.-106G>T | upstream_gene_variant | 0.22 |
mshA | 575283 | c.-65C>A | upstream_gene_variant | 0.29 |
mshA | 576071 | p.Val242Ile | missense_variant | 0.25 |
ccsA | 620057 | p.Thr56Ser | missense_variant | 0.22 |
ccsA | 620198 | p.Gln103Arg | missense_variant | 0.12 |
ccsA | 620309 | c.421delC | frameshift_variant | 0.18 |
rpoB | 760400 | c.594G>A | synonymous_variant | 0.15 |
rpoB | 762461 | p.Asn885Lys | missense_variant | 0.22 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.33 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.5 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.5 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.5 |
rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.5 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.47 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.45 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.54 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.42 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.32 |
rpoC | 764093 | p.Arg242Cys | missense_variant | 0.25 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.27 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.31 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.31 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.31 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.36 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.52 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.52 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.71 |
rpoC | 764641 | c.1272C>T | synonymous_variant | 0.69 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.6 |
rpoC | 764663 | p.Val432Thr | missense_variant | 0.33 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.3 |
rpoC | 764672 | p.Gln435Glu | missense_variant | 0.3 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.3 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.2 |
rpoC | 765446 | p.Gln693* | stop_gained | 0.13 |
rpoC | 766297 | c.2928G>T | synonymous_variant | 0.33 |
rpoC | 767161 | c.3792C>A | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776847 | p.Gln545Arg | missense_variant | 0.22 |
mmpL5 | 777579 | p.Thr301Asn | missense_variant | 0.33 |
mmpL5 | 777764 | c.717G>T | synonymous_variant | 0.14 |
mmpL5 | 778368 | p.Gly38Ala | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781525 | c.-35A>T | upstream_gene_variant | 0.14 |
rplC | 801054 | c.246G>A | synonymous_variant | 0.22 |
fbiC | 1303610 | p.Gly227Glu | missense_variant | 0.12 |
fbiC | 1304094 | p.Met388Ile | missense_variant | 0.14 |
fbiC | 1305447 | c.2517C>A | synonymous_variant | 0.13 |
Rv1258c | 1406613 | p.Glu243Gly | missense_variant | 0.14 |
Rv1258c | 1407529 | c.-189T>C | upstream_gene_variant | 0.12 |
embR | 1416364 | c.984C>T | synonymous_variant | 0.17 |
embR | 1416724 | p.Trp208Cys | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471876 | n.31G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1471892 | n.47G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472264 | n.419T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472284 | n.439C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472303 | n.458G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472333 | n.488G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472338 | n.493A>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472349 | n.504A>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472382 | n.537G>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472415 | n.570T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472499 | n.654A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472715 | n.870C>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472770 | n.925C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472826 | n.981G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473223 | n.1378G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473352 | n.1507C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473353 | n.1508C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473358 | n.1513G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473359 | n.1514G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474922 | n.1265G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475091 | n.1434G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475790 | n.2133C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476491 | n.2834T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.18 |
inhA | 1673718 | c.-484G>A | upstream_gene_variant | 0.18 |
fabG1 | 1673915 | p.Gly159Ala | missense_variant | 0.13 |
fabG1 | 1674143 | p.Ala235Val | missense_variant | 0.22 |
inhA | 1674350 | p.Ile50Thr | missense_variant | 0.12 |
rpsA | 1833374 | c.-168C>T | upstream_gene_variant | 0.12 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.4 |
rpsA | 1834435 | c.894G>T | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101788 | p.Val419Leu | missense_variant | 0.14 |
ndh | 2101903 | c.1140C>A | synonymous_variant | 0.25 |
ndh | 2102293 | c.750C>T | synonymous_variant | 0.15 |
ndh | 2103143 | c.-101G>T | upstream_gene_variant | 0.4 |
katG | 2153933 | p.Ala727Thr | missense_variant | 0.25 |
katG | 2154555 | c.1557C>A | synonymous_variant | 0.25 |
katG | 2155265 | p.Leu283Met | missense_variant | 0.5 |
Rv1979c | 2223233 | c.-69G>A | upstream_gene_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289209 | c.33C>T | synonymous_variant | 0.2 |
pncA | 2289824 | c.-583T>A | upstream_gene_variant | 0.2 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 0.33 |
eis | 2714640 | c.693C>T | synonymous_variant | 0.17 |
eis | 2714890 | p.Arg148Leu | missense_variant | 0.14 |
ahpC | 2726333 | p.Trp47Cys | missense_variant | 0.11 |
folC | 2746250 | p.Ala450Asp | missense_variant | 0.25 |
folC | 2747143 | c.456C>T | synonymous_variant | 0.13 |
pepQ | 2859847 | p.Glu191Val | missense_variant | 0.17 |
pepQ | 2860176 | c.243C>A | synonymous_variant | 0.5 |
pepQ | 2860466 | c.-48C>T | upstream_gene_variant | 0.17 |
ribD | 2987516 | c.678C>A | synonymous_variant | 0.17 |
Rv2752c | 3064654 | p.Ala513Val | missense_variant | 0.29 |
Rv2752c | 3065086 | p.Arg369Met | missense_variant | 0.29 |
ald | 3086744 | c.-76A>G | upstream_gene_variant | 0.18 |
ald | 3087600 | p.Gly261Cys | missense_variant | 0.14 |
fbiD | 3339119 | c.2T>C | start_lost | 0.29 |
Rv3083 | 3448480 | c.-24G>A | upstream_gene_variant | 0.22 |
Rv3083 | 3448525 | c.22C>T | synonymous_variant | 0.12 |
Rv3083 | 3449477 | p.Thr325Asn | missense_variant | 0.17 |
fprA | 3473874 | c.-132delG | upstream_gene_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474968 | p.Ser321Leu | missense_variant | 0.4 |
Rv3236c | 3612151 | c.966G>T | synonymous_variant | 0.18 |
Rv3236c | 3612499 | c.618C>T | synonymous_variant | 0.22 |
fbiA | 3640745 | p.Thr68Ile | missense_variant | 0.25 |
fbiA | 3640909 | p.Tyr123His | missense_variant | 0.2 |
fbiA | 3640934 | p.Ala131Val | missense_variant | 0.22 |
alr | 3840267 | p.Thr385Ile | missense_variant | 0.18 |
ddn | 3986930 | c.87C>T | synonymous_variant | 0.22 |
ddn | 3986958 | p.Gly39Cys | missense_variant | 0.17 |
clpC1 | 4039496 | p.Ile403Met | missense_variant | 0.23 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.21 |
clpC1 | 4039533 | p.Asn391Thr | missense_variant | 0.27 |
clpC1 | 4039546 | p.Asp387Asn | missense_variant | 0.17 |
clpC1 | 4039549 | p.Ala386Ser | missense_variant | 0.17 |
clpC1 | 4039640 | c.1065C>G | synonymous_variant | 0.67 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.67 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.4 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.33 |
clpC1 | 4039667 | p.Gln346Phe | missense_variant | 0.29 |
clpC1 | 4039673 | c.1032G>A | synonymous_variant | 0.22 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.25 |
clpC1 | 4039690 | p.Glu339Gln | missense_variant | 0.33 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.33 |
clpC1 | 4039697 | c.1008C>G | synonymous_variant | 0.33 |
clpC1 | 4039711 | p.Ile332Val | missense_variant | 0.42 |
clpC1 | 4039712 | c.993C>T | synonymous_variant | 0.42 |
clpC1 | 4039718 | c.987C>T | synonymous_variant | 0.38 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.18 |
clpC1 | 4040580 | c.124delG | frameshift_variant | 0.2 |
embC | 4241284 | c.1422G>A | synonymous_variant | 0.18 |
embC | 4241504 | p.Val548Leu | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244701 | p.Gly490Val | missense_variant | 0.2 |
embB | 4247673 | p.Ala387Glu | missense_variant | 0.25 |
embB | 4248050 | p.Gly513Trp | missense_variant | 0.25 |
embB | 4248579 | p.Ala689Val | missense_variant | 0.2 |
embB | 4248766 | c.2253C>T | synonymous_variant | 0.15 |
aftB | 4268353 | p.Leu162Val | missense_variant | 0.13 |
aftB | 4269153 | c.-317C>T | upstream_gene_variant | 0.22 |
ethA | 4328329 | c.-856C>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407661 | p.Ser181Leu | missense_variant | 0.15 |