Run ID: SRR4033481
Sample name:
Date: 04-04-2023 06:07:29
Number of reads: 892860
Percentage reads mapped: 99.6
Strain: lineage4.3.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.99 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 0.98 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gid | 4407830 | p.Gln125* | stop_gained | 0.15 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrB | 5909 | p.Ser224Cys | missense_variant | 0.18 |
gyrB | 6049 | c.810G>C | synonymous_variant | 0.11 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7342 | p.Arg14Pro | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7648 | p.Phe116Tyr | missense_variant | 0.18 |
gyrA | 8376 | p.Asp359Asn | missense_variant | 0.12 |
gyrA | 8926 | p.Lys542Arg | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9312 | p.Leu671Val | missense_variant | 0.11 |
gyrA | 9616 | p.Ser772Thr | missense_variant | 0.14 |
gyrA | 9705 | p.Arg802Trp | missense_variant | 0.12 |
fgd1 | 490633 | c.-149delA | upstream_gene_variant | 0.14 |
fgd1 | 491764 | c.982C>T | synonymous_variant | 0.15 |
mshA | 576542 | p.Ala399Thr | missense_variant | 0.14 |
mshA | 576754 | c.1407C>T | synonymous_variant | 0.15 |
ccsA | 619840 | c.-51G>A | upstream_gene_variant | 0.14 |
rpoB | 760513 | p.Gly236Asp | missense_variant | 0.18 |
rpoB | 761177 | c.1371G>T | synonymous_variant | 0.17 |
rpoB | 762106 | p.Ile767Asn | missense_variant | 0.13 |
rpoB | 763111 | c.3308delG | frameshift_variant | 0.15 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.96 |
rpoC | 766456 | c.3087C>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776239 | p.Gly748Arg | missense_variant | 0.15 |
mmpL5 | 776359 | p.Phe708Ile | missense_variant | 0.17 |
mmpL5 | 777844 | p.Thr213Ala | missense_variant | 0.13 |
mmpR5 | 779071 | p.Glu28* | stop_gained | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781401 | c.-159T>A | upstream_gene_variant | 0.2 |
fbiC | 1303458 | c.528G>C | synonymous_variant | 0.2 |
fbiC | 1304429 | p.Arg500Gln | missense_variant | 0.14 |
Rv1258c | 1406270 | c.1071C>T | synonymous_variant | 0.13 |
Rv1258c | 1406350 | p.Ile331Phe | missense_variant | 0.17 |
Rv1258c | 1406727 | p.Pro205His | missense_variant | 0.18 |
Rv1258c | 1406952 | p.Glu130Val | missense_variant | 0.22 |
Rv1258c | 1406967 | p.Asp125Val | missense_variant | 0.2 |
Rv1258c | 1407186 | p.Met52Lys | missense_variant | 0.18 |
atpE | 1461047 | c.3G>A | start_lost | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471696 | n.-150T>C | upstream_gene_variant | 0.14 |
rrs | 1472042 | n.197T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472891 | n.1046A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472968 | n.1123C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475268 | n.1611T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475793 | n.2136T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476201 | n.2544C>G | non_coding_transcript_exon_variant | 0.18 |
inhA | 1674337 | c.136C>T | synonymous_variant | 0.2 |
inhA | 1674346 | p.Arg49Cys | missense_variant | 0.22 |
inhA | 1674736 | p.Ala179Thr | missense_variant | 0.14 |
inhA | 1674744 | c.543G>A | synonymous_variant | 0.15 |
rpsA | 1833625 | p.Lys28Asn | missense_variant | 0.14 |
rpsA | 1833642 | p.Asn34Ser | missense_variant | 0.14 |
rpsA | 1834906 | c.1365G>C | synonymous_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918359 | c.420A>T | synonymous_variant | 0.14 |
ndh | 2101959 | c.1083delA | frameshift_variant | 0.13 |
katG | 2154469 | p.Gly548Asp | missense_variant | 0.17 |
katG | 2155082 | p.Thr344Ala | missense_variant | 0.12 |
katG | 2155664 | p.Pro150Thr | missense_variant | 0.13 |
katG | 2156104 | p.Glu3Val | missense_variant | 0.13 |
katG | 2156523 | c.-412G>A | upstream_gene_variant | 0.18 |
PPE35 | 2167878 | p.Ser912Thr | missense_variant | 0.12 |
PPE35 | 2168172 | p.Ile814Thr | missense_variant | 0.11 |
PPE35 | 2168257 | p.Leu786Met | missense_variant | 0.13 |
PPE35 | 2168650 | p.Val655Met | missense_variant | 0.12 |
PPE35 | 2168828 | c.1785G>C | synonymous_variant | 0.11 |
PPE35 | 2169261 | p.Leu451Pro | missense_variant | 0.13 |
PPE35 | 2169607 | p.Asn336Asp | missense_variant | 0.11 |
PPE35 | 2170049 | c.563dupC | frameshift_variant | 0.5 |
Rv1979c | 2222475 | c.690C>T | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288942 | c.300C>A | synonymous_variant | 0.13 |
pncA | 2289383 | c.-142G>T | upstream_gene_variant | 0.14 |
pncA | 2290039 | c.-798C>T | upstream_gene_variant | 0.12 |
kasA | 2518610 | c.500delC | frameshift_variant | 0.17 |
kasA | 2518739 | p.Ala209Pro | missense_variant | 0.14 |
eis | 2714339 | p.Lys332Glu | missense_variant | 0.18 |
eis | 2714774 | p.Pro187Ala | missense_variant | 0.12 |
eis | 2715230 | p.Ala35Thr | missense_variant | 0.18 |
ahpC | 2726040 | c.-153G>A | upstream_gene_variant | 0.15 |
ahpC | 2726774 | c.582G>A | synonymous_variant | 0.22 |
folC | 2747544 | p.Pro19Ser | missense_variant | 0.17 |
Rv2752c | 3064671 | c.1521C>G | synonymous_variant | 0.11 |
Rv2752c | 3065888 | p.Val102Ile | missense_variant | 0.12 |
Rv2752c | 3066315 | c.-124C>T | upstream_gene_variant | 0.22 |
Rv2752c | 3067126 | c.-935C>T | upstream_gene_variant | 0.5 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.25 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.83 |
thyA | 3074326 | p.Lys49Ile | missense_variant | 0.15 |
ald | 3086757 | c.-63G>T | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087150 | p.Gly111Ser | missense_variant | 0.14 |
ald | 3087355 | p.Ala179Asp | missense_variant | 0.15 |
ald | 3087652 | p.Ser278Leu | missense_variant | 0.14 |
Rv3083 | 3448524 | c.21C>A | synonymous_variant | 0.14 |
Rv3083 | 3449895 | p.Met464Ile | missense_variant | 0.17 |
Rv3083 | 3449911 | p.Ala470Thr | missense_variant | 0.17 |
fprA | 3473839 | c.-168G>A | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474322 | p.Ala106Thr | missense_variant | 0.25 |
whiB7 | 3568547 | p.Ser45Gly | missense_variant | 0.15 |
whiB7 | 3568836 | c.-157A>G | upstream_gene_variant | 0.2 |
Rv3236c | 3612902 | p.Ala72Val | missense_variant | 0.13 |
fbiA | 3640497 | c.-46G>A | upstream_gene_variant | 0.12 |
fbiA | 3640757 | p.Gly72Glu | missense_variant | 0.17 |
fbiA | 3640771 | p.Arg77Cys | missense_variant | 0.18 |
fbiB | 3642506 | p.Asp324Glu | missense_variant | 0.13 |
fbiB | 3642670 | p.Ala379Val | missense_variant | 0.14 |
alr | 3840648 | p.Tyr258Phe | missense_variant | 0.17 |
alr | 3840752 | c.669C>A | synonymous_variant | 0.17 |
alr | 3841081 | p.His114Tyr | missense_variant | 0.13 |
rpoA | 3877683 | c.825G>T | synonymous_variant | 0.18 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.95 |
clpC1 | 4038920 | p.Phe595Leu | missense_variant | 0.15 |
clpC1 | 4039108 | c.1597C>A | synonymous_variant | 0.14 |
clpC1 | 4039115 | c.1589_1590insT | frameshift_variant | 0.17 |
embC | 4240043 | p.Trp61Arg | missense_variant | 0.18 |
embC | 4240286 | p.Ala142Thr | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243137 | p.Arg1092Leu | missense_variant | 0.15 |
embA | 4243557 | p.Ala109Thr | missense_variant | 0.13 |
embA | 4243877 | c.645G>T | synonymous_variant | 0.12 |
embA | 4243989 | p.Ala253Thr | missense_variant | 0.29 |
embA | 4244163 | p.Leu311Ile | missense_variant | 0.17 |
embA | 4245801 | p.Tyr857His | missense_variant | 0.13 |
embB | 4245807 | c.-707T>C | upstream_gene_variant | 0.17 |
embB | 4247828 | p.Ala439Thr | missense_variant | 0.13 |
embB | 4248208 | p.Ser565Arg | missense_variant | 0.12 |
embB | 4248383 | p.Asn624Asp | missense_variant | 0.12 |
embB | 4248923 | p.Met804Val | missense_variant | 0.11 |
embB | 4249704 | p.Leu1064Gln | missense_variant | 0.12 |
embB | 4249714 | c.3201C>T | synonymous_variant | 0.14 |
aftB | 4268047 | p.Tyr264His | missense_variant | 0.15 |
aftB | 4268333 | c.504C>T | synonymous_variant | 0.15 |
ethA | 4326209 | p.Pro422Arg | missense_variant | 0.13 |
ethA | 4326496 | c.978G>T | synonymous_variant | 0.2 |
ethA | 4326539 | p.Val312Ala | missense_variant | 0.14 |
whiB6 | 4338206 | p.Val106Met | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.25 |
gid | 4407620 | p.Tyr195His | missense_variant | 0.17 |
gid | 4407851 | p.Arg118Cys | missense_variant | 0.15 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408311 | c.-109C>A | upstream_gene_variant | 0.15 |
gid | 4408411 | c.-209G>A | upstream_gene_variant | 0.15 |