Run ID: SRR12830387
Sample name:
Date: 03-04-2023 06:58:57
Number of reads: 439389
Percentage reads mapped: 99.78
Strain: lineage4.3.3
Drug-resistance: Sensitive
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 | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5474 | p.Asp79Asn | missense_variant | 0.13 |
gyrB | 5527 | c.288C>T | synonymous_variant | 0.12 |
gyrB | 5562 | p.Lys108Arg | missense_variant | 0.12 |
gyrB | 6608 | p.Val457Phe | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9651 | p.Ile784Val | missense_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766711 | c.3342C>A | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776372 | c.2109C>A | synonymous_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304519 | p.Ala530Glu | missense_variant | 0.13 |
Rv1258c | 1406597 | c.744G>T | synonymous_variant | 0.13 |
Rv1258c | 1406863 | p.Ile160Phe | missense_variant | 0.25 |
embR | 1416980 | p.Val123Gly | missense_variant | 0.2 |
embR | 1417511 | c.-164C>G | upstream_gene_variant | 0.11 |
embR | 1417521 | c.-175delC | upstream_gene_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474059 | n.402C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833942 | p.Val134Ala | missense_variant | 0.11 |
rpsA | 1834568 | p.Asp343Tyr | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102308 | c.735G>A | synonymous_variant | 1.0 |
katG | 2154239 | p.Thr625Ser | missense_variant | 0.17 |
katG | 2154661 | p.Arg484His | missense_variant | 0.12 |
PPE35 | 2170263 | p.Leu117Pro | missense_variant | 1.0 |
Rv1979c | 2223056 | c.108delA | frameshift_variant | 0.14 |
Rv1979c | 2223167 | c.-3G>T | upstream_gene_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518736 | p.Ala208Thr | missense_variant | 0.14 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2714313 | p.Cys340* | stop_gained | 0.2 |
eis | 2714475 | c.858C>T | synonymous_variant | 0.14 |
eis | 2714958 | c.375C>A | synonymous_variant | 0.12 |
folC | 2747520 | p.Leu27Met | missense_variant | 0.17 |
thyX | 3067436 | c.510C>T | synonymous_variant | 0.15 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074297 | p.Leu59Met | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087311 | c.492C>T | synonymous_variant | 0.12 |
ald | 3087706 | p.Tyr296Phe | missense_variant | 0.14 |
ald | 3087767 | c.948G>C | synonymous_variant | 0.13 |
Rv3083 | 3449563 | p.Gly354Ser | missense_variant | 0.27 |
Rv3083 | 3449854 | p.Met451Val | missense_variant | 1.0 |
Rv3083 | 3449865 | c.1362G>A | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612255 | p.Val288Ile | missense_variant | 0.12 |
Rv3236c | 3612479 | p.Pro213Leu | missense_variant | 0.12 |
fbiA | 3640636 | p.Ser32Thr | missense_variant | 0.2 |
fbiB | 3642496 | p.Leu321Pro | missense_variant | 0.1 |
alr | 3841553 | c.-133G>T | upstream_gene_variant | 0.17 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039252 | p.Ala485Ser | missense_variant | 0.15 |
clpC1 | 4039306 | p.Gln467Lys | missense_variant | 0.13 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.15 |
embC | 4241882 | c.2020C>T | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246787 | p.Pro92Thr | missense_variant | 0.14 |
embB | 4248849 | p.Pro779Gln | missense_variant | 0.14 |
aftB | 4268083 | p.Gln252* | stop_gained | 0.17 |
aftB | 4268697 | p.Pro47Leu | missense_variant | 0.13 |
aftB | 4268763 | p.Arg25His | missense_variant | 0.12 |
aftB | 4269282 | c.-446G>A | upstream_gene_variant | 0.18 |
ubiA | 4269713 | p.Gly41Cys | missense_variant | 0.12 |
ethA | 4326401 | p.Gly358Val | missense_variant | 0.14 |
ethA | 4327578 | c.-105C>A | upstream_gene_variant | 0.18 |
whiB6 | 4338194 | c.328C>A | synonymous_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407955 | p.Arg83Gln | missense_variant | 0.13 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |