Run ID: ERR2229411
Sample name:
Date: 31-03-2023 17:10:05
Number of reads: 376512
Percentage reads mapped: 99.2
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7347 | p.Glu16Lys | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8089 | p.Ser263Tyr | missense_variant | 0.29 |
gyrA | 8864 | c.1563C>A | synonymous_variant | 0.15 |
mshA | 575527 | c.180G>T | synonymous_variant | 0.15 |
mshA | 576674 | p.Arg443Ser | missense_variant | 0.29 |
ccsA | 620539 | p.Arg217Gly | missense_variant | 0.4 |
rpoC | 764237 | p.Leu290Ile | missense_variant | 0.17 |
rpoC | 764601 | p.Gly411Ala | missense_variant | 0.2 |
rpoC | 765124 | c.1755G>T | synonymous_variant | 0.18 |
rpoC | 765217 | c.1848C>T | synonymous_variant | 0.2 |
rpoC | 766406 | p.Arg1013Ser | missense_variant | 0.22 |
rpoC | 767276 | p.Ala1303Ser | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781765 | p.Gly69Val | missense_variant | 0.15 |
rplC | 800689 | c.-120G>A | upstream_gene_variant | 0.17 |
fbiC | 1303051 | p.Val41Met | missense_variant | 0.17 |
fbiC | 1303168 | p.Gly80Cys | missense_variant | 0.12 |
fbiC | 1303213 | p.Thr95Ala | missense_variant | 0.17 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407005 | p.Leu112Arg | missense_variant | 0.2 |
Rv1258c | 1407059 | p.Trp94Cys | missense_variant | 0.25 |
embR | 1416808 | c.540C>A | synonymous_variant | 0.12 |
embR | 1417063 | c.285C>T | synonymous_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471953 | n.108G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474908 | n.1251G>T | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673374 | c.-66C>A | upstream_gene_variant | 0.22 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918367 | p.Ala143Val | missense_variant | 0.14 |
ndh | 2103135 | c.-93A>G | upstream_gene_variant | 0.4 |
PPE35 | 2168485 | p.Asn710Tyr | missense_variant | 0.25 |
PPE35 | 2168517 | c.2095delA | frameshift_variant | 0.25 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.14 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.15 |
PPE35 | 2169695 | c.918A>G | synonymous_variant | 0.12 |
PPE35 | 2169703 | p.Asn304Asp | missense_variant | 0.11 |
PPE35 | 2169704 | c.909A>C | synonymous_variant | 0.11 |
PPE35 | 2169707 | p.Thr302Ser | missense_variant | 0.12 |
PPE35 | 2169717 | p.Asn299Ile | missense_variant | 0.18 |
PPE35 | 2169875 | c.738T>C | synonymous_variant | 0.11 |
PPE35 | 2169884 | c.729T>C | synonymous_variant | 0.11 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.11 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.12 |
PPE35 | 2170169 | c.444A>G | synonymous_variant | 0.12 |
Rv1979c | 2223049 | p.Val39Ala | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714464 | p.Arg290His | missense_variant | 0.22 |
ahpC | 2726276 | c.84C>A | synonymous_variant | 0.17 |
folC | 2746965 | p.Ile212Phe | missense_variant | 0.22 |
ribD | 2987350 | p.Gly171Ala | missense_variant | 0.4 |
Rv2752c | 3067063 | c.-872C>T | upstream_gene_variant | 0.18 |
thyX | 3067410 | p.Thr179Ile | missense_variant | 0.17 |
thyA | 3074565 | c.-94C>T | upstream_gene_variant | 0.33 |
thyA | 3074580 | c.-109T>C | upstream_gene_variant | 0.33 |
thyA | 3074637 | c.-166A>G | upstream_gene_variant | 0.5 |
fbiD | 3339350 | p.Asp78Gly | missense_variant | 0.15 |
fbiD | 3339354 | c.237A>G | synonymous_variant | 0.15 |
fbiD | 3339510 | c.393C>A | synonymous_variant | 0.22 |
Rv3083 | 3448346 | c.-158C>A | upstream_gene_variant | 0.14 |
fprA | 3474254 | p.Val83Asp | missense_variant | 0.17 |
fprA | 3474766 | p.Gly254Ser | missense_variant | 0.18 |
fbiB | 3641205 | c.-330C>A | upstream_gene_variant | 0.2 |
fbiA | 3641411 | p.Val290Ala | missense_variant | 0.15 |
fbiB | 3642876 | p.Lys448Glu | missense_variant | 0.29 |
alr | 3840491 | c.930G>T | synonymous_variant | 0.2 |
alr | 3841582 | c.-162A>G | upstream_gene_variant | 0.12 |
alr | 3841589 | c.-170delG | upstream_gene_variant | 0.12 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.3 |
clpC1 | 4039530 | p.Asp392Ala | missense_variant | 0.33 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.11 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.17 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.2 |
clpC1 | 4040878 | c.-174T>G | upstream_gene_variant | 0.21 |
embC | 4240987 | c.1125G>T | synonymous_variant | 0.5 |
embC | 4241254 | c.1392C>T | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243516 | p.Ala95Asp | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407627 | c.576C>T | synonymous_variant | 0.17 |
gid | 4407775 | p.Asp143Val | missense_variant | 0.14 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |