Run ID: SRR4035801
Sample name:
Date: 04-04-2023 07:18:27
Number of reads: 1643750
Percentage reads mapped: 99.38
Strain: lineage4.1.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gid | 4408137 | p.Tyr22* | stop_gained | 0.12 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5470 | c.231C>T | synonymous_variant | 0.13 |
gyrB | 5520 | p.Pro94Arg | missense_variant | 0.18 |
gyrA | 7318 | p.Leu6* | stop_gained | 0.14 |
gyrA | 7327 | p.Asp9Gly | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7717 | p.Met139Thr | missense_variant | 0.11 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491278 | p.Pro166Ser | missense_variant | 0.17 |
fgd1 | 491285 | p.Gly168Val | missense_variant | 0.17 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.94 |
mshA | 575220 | c.-128G>C | upstream_gene_variant | 0.11 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.15 |
mshA | 576389 | p.Val348Leu | missense_variant | 0.15 |
mshA | 576458 | p.Ala371Pro | missense_variant | 0.15 |
mshA | 576616 | c.1269G>T | synonymous_variant | 0.15 |
mshA | 576631 | c.1284C>T | synonymous_variant | 0.17 |
ccsA | 620376 | c.486G>T | synonymous_variant | 0.17 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761029 | p.Pro408Arg | missense_variant | 0.11 |
rpoB | 761538 | p.Arg578Cys | missense_variant | 0.15 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.11 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.9 |
rpoC | 767131 | p.Ile1254Met | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpR5 | 778001 | c.-989T>C | upstream_gene_variant | 0.12 |
mmpL5 | 778120 | p.Thr121Ala | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303224 | c.294C>T | synonymous_variant | 0.12 |
fbiC | 1304433 | c.1503G>C | synonymous_variant | 0.12 |
fbiC | 1304439 | p.Glu503Asp | missense_variant | 0.11 |
fbiC | 1304526 | c.1596T>C | synonymous_variant | 0.12 |
fbiC | 1304537 | p.Arg536Pro | missense_variant | 0.13 |
fbiC | 1304551 | p.Gly541Ser | missense_variant | 0.13 |
fbiC | 1304823 | p.His631Gln | missense_variant | 0.14 |
fbiC | 1305079 | p.Arg717Gly | missense_variant | 0.25 |
fbiC | 1305088 | p.Val720Leu | missense_variant | 0.25 |
fbiC | 1305103 | p.Val725Met | missense_variant | 0.17 |
Rv1258c | 1406458 | p.Val295Ile | missense_variant | 0.15 |
Rv1258c | 1406979 | c.358_361delGGCA | frameshift_variant | 0.18 |
Rv1258c | 1407288 | p.Met18Lys | missense_variant | 0.15 |
Rv1258c | 1407304 | p.Leu13Val | missense_variant | 0.13 |
embR | 1416619 | c.729C>A | synonymous_variant | 0.14 |
embR | 1416628 | c.720C>G | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474909 | n.1252C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474930 | n.1273A>G | non_coding_transcript_exon_variant | 0.11 |
inhA | 1674410 | p.His70Arg | missense_variant | 0.11 |
rpsA | 1833383 | c.-159C>T | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917982 | p.Gly15Ser | missense_variant | 0.14 |
tlyA | 1918696 | p.Ala253Ser | missense_variant | 0.12 |
ndh | 2102154 | p.Leu297Phe | missense_variant | 0.14 |
katG | 2154432 | c.1680C>G | synonymous_variant | 0.13 |
katG | 2155481 | p.Ser211Arg | missense_variant | 0.11 |
katG | 2155970 | p.Leu48Val | missense_variant | 0.12 |
katG | 2155994 | p.Pro40Ser | missense_variant | 0.17 |
katG | 2156436 | c.-325C>A | upstream_gene_variant | 0.16 |
PPE35 | 2169121 | p.Val498Leu | missense_variant | 0.11 |
PPE35 | 2169182 | c.1431G>A | synonymous_variant | 0.14 |
PPE35 | 2169443 | c.1170T>C | synonymous_variant | 0.11 |
PPE35 | 2170352 | c.261C>A | synonymous_variant | 0.18 |
PPE35 | 2170415 | c.198A>T | synonymous_variant | 0.25 |
PPE35 | 2170483 | p.Ser44Ala | missense_variant | 0.1 |
Rv1979c | 2222545 | p.Leu207Ser | missense_variant | 0.1 |
Rv1979c | 2222659 | p.Gly169Asp | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289447 | c.-206G>C | upstream_gene_variant | 0.11 |
pncA | 2289863 | c.-623_-622delAGinsGA | upstream_gene_variant | 0.13 |
pncA | 2290007 | c.-766A>G | upstream_gene_variant | 0.11 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2519331 | p.Gly406Asp | missense_variant | 0.15 |
folC | 2746551 | p.Ile350Val | missense_variant | 0.18 |
folC | 2746578 | p.Arg341Cys | missense_variant | 0.13 |
folC | 2746611 | p.Phe330Leu | missense_variant | 0.11 |
folC | 2746707 | p.Gln298* | stop_gained | 0.13 |
pepQ | 2859879 | p.Met180Ile | missense_variant | 0.13 |
pepQ | 2860164 | c.255C>G | synonymous_variant | 0.12 |
ribD | 2986656 | c.-183A>G | upstream_gene_variant | 0.11 |
ribD | 2987336 | c.498C>A | synonymous_variant | 0.15 |
ribD | 2987569 | p.Leu244His | missense_variant | 0.2 |
Rv2752c | 3065598 | c.594G>T | synonymous_variant | 0.12 |
thyX | 3067288 | p.Ala220Thr | missense_variant | 0.17 |
thyX | 3067509 | p.Leu146Gln | missense_variant | 0.13 |
thyX | 3068040 | c.-95C>A | upstream_gene_variant | 0.15 |
thyX | 3068081 | c.-136A>G | upstream_gene_variant | 0.15 |
thyA | 3074404 | p.Gly23Asp | missense_variant | 0.12 |
thyA | 3074510 | c.-39C>A | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087873 | p.Ser352Pro | missense_variant | 0.13 |
Rv3083 | 3448704 | c.201C>T | synonymous_variant | 0.12 |
Rv3083 | 3449405 | p.Pro301Leu | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3612021 | p.Gly366Arg | missense_variant | 0.18 |
fbiA | 3640546 | p.Lys2Glu | missense_variant | 0.13 |
fbiA | 3641116 | p.Lys192Glu | missense_variant | 0.12 |
fbiA | 3641129 | p.Ala196Val | missense_variant | 0.2 |
fbiB | 3641917 | p.Ser128Thr | missense_variant | 0.17 |
fbiB | 3642274 | p.Glu247Gly | missense_variant | 0.12 |
alr | 3841117 | p.Ala102Thr | missense_variant | 0.17 |
alr | 3841378 | p.Thr15Ser | missense_variant | 0.14 |
alr | 3841385 | c.36C>T | synonymous_variant | 0.14 |
rpoA | 3878092 | p.Val139Ala | missense_variant | 0.12 |
ddn | 3986933 | c.90C>T | synonymous_variant | 0.13 |
ddn | 3986977 | p.Pro45Leu | missense_variant | 0.13 |
clpC1 | 4039242 | p.Leu488Pro | missense_variant | 0.11 |
clpC1 | 4040235 | p.Gly157Ala | missense_variant | 0.15 |
embC | 4240223 | c.361C>T | synonymous_variant | 0.14 |
embC | 4240238 | p.Ala126Thr | missense_variant | 0.13 |
embC | 4241002 | c.1140G>A | synonymous_variant | 0.13 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.14 |
embC | 4241754 | p.Ala631Val | missense_variant | 0.24 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242725 | p.Gln955Lys | missense_variant | 0.12 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243983 | c.751C>A | synonymous_variant | 0.13 |
embA | 4244097 | p.Tyr289Asn | missense_variant | 0.13 |
embA | 4244879 | c.1647C>A | synonymous_variant | 0.15 |
embA | 4244900 | c.1668G>C | synonymous_variant | 0.2 |
embB | 4246049 | c.-465G>A | upstream_gene_variant | 0.15 |
embB | 4246722 | p.Pro70Gln | missense_variant | 0.2 |
embB | 4248392 | c.1880delC | frameshift_variant | 0.14 |
embB | 4249650 | p.Ala1046Val | missense_variant | 0.18 |
embB | 4249659 | p.Met1049Lys | missense_variant | 0.2 |
embB | 4249668 | p.Tyr1052Cys | missense_variant | 0.2 |
aftB | 4267821 | p.Leu339Ser | missense_variant | 0.15 |
aftB | 4268335 | p.Ser168Gly | missense_variant | 0.13 |
aftB | 4268366 | p.Cys157Trp | missense_variant | 0.12 |
aftB | 4268384 | c.453G>A | synonymous_variant | 0.13 |
aftB | 4269108 | c.-272C>G | upstream_gene_variant | 0.1 |
ethA | 4327578 | c.-105C>G | upstream_gene_variant | 0.11 |
whiB6 | 4338244 | p.Gly93Val | missense_variant | 0.12 |
whiB6 | 4338443 | p.Tyr27His | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408119 | c.84A>G | synonymous_variant | 0.15 |
gid | 4408228 | c.-26G>A | upstream_gene_variant | 0.14 |
gid | 4408397 | c.-195A>G | upstream_gene_variant | 0.14 |