Run ID: ERR2229316
Sample name:
Date: 31-03-2023 17:00:12
Number of reads: 713016
Percentage reads mapped: 95.42
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7194 | p.Met652Thr | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7822 | p.Leu174Arg | missense_variant | 0.22 |
gyrA | 7883 | c.582G>T | synonymous_variant | 0.15 |
fgd1 | 491099 | p.Gly106Val | missense_variant | 0.17 |
fgd1 | 491639 | p.Val286Ala | missense_variant | 0.2 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.15 |
rpoC | 763912 | c.543G>C | synonymous_variant | 0.2 |
rpoC | 764148 | p.Ser260* | stop_gained | 0.29 |
rpoC | 765260 | p.Ala631Thr | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775871 | c.2610C>T | synonymous_variant | 0.33 |
mmpL5 | 775874 | c.2607C>A | synonymous_variant | 0.38 |
mmpL5 | 776087 | c.2394C>G | synonymous_variant | 0.33 |
mmpL5 | 776510 | c.1971C>A | synonymous_variant | 0.25 |
mmpR5 | 778328 | c.-662C>T | upstream_gene_variant | 0.17 |
mmpS5 | 778482 | p.Ala142Ser | missense_variant | 0.14 |
mmpL5 | 778872 | c.-392C>T | upstream_gene_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781665 | p.Arg36Cys | missense_variant | 0.12 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.14 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304296 | p.Gln456* | stop_gained | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.17 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.26 |
rpsA | 1833960 | p.Leu140Pro | missense_variant | 0.29 |
rpsA | 1834757 | p.Gly406* | stop_gained | 0.22 |
rpsA | 1834795 | p.Tyr418* | stop_gained | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918296 | c.357G>T | synonymous_variant | 0.15 |
ndh | 2101769 | p.Arg425Leu | missense_variant | 0.12 |
ndh | 2101827 | p.Gly406Trp | missense_variant | 0.2 |
ndh | 2102264 | p.Lys260Arg | missense_variant | 0.15 |
katG | 2155378 | p.Ala245Glu | missense_variant | 0.17 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.2 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.2 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168871 | p.Leu581Pro | missense_variant | 0.17 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.52 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.47 |
PPE35 | 2170189 | p.Glu142Gln | missense_variant | 0.14 |
PPE35 | 2170403 | c.210C>G | synonymous_variant | 0.19 |
PPE35 | 2170406 | c.207A>G | synonymous_variant | 0.19 |
Rv1979c | 2223278 | c.-114G>C | upstream_gene_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518403 | p.Ser97Thr | missense_variant | 0.14 |
eis | 2714324 | p.Arg337Ser | missense_variant | 0.14 |
eis | 2715424 | c.-92C>T | upstream_gene_variant | 0.13 |
ahpC | 2725995 | c.-198A>G | upstream_gene_variant | 0.13 |
pepQ | 2859604 | p.Gly272Glu | missense_variant | 0.18 |
pepQ | 2859791 | p.Ala210Thr | missense_variant | 0.25 |
thyX | 3067837 | p.Glu37* | stop_gained | 0.2 |
thyX | 3067863 | p.Asp28Gly | missense_variant | 0.29 |
thyA | 3073803 | c.669G>A | synonymous_variant | 0.12 |
thyA | 3074238 | c.234C>A | synonymous_variant | 0.2 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
whiB7 | 3568877 | c.-198C>T | upstream_gene_variant | 0.18 |
Rv3236c | 3611962 | c.1155C>T | synonymous_variant | 0.15 |
fbiA | 3640365 | c.-178C>T | upstream_gene_variant | 0.17 |
fbiB | 3641223 | c.-312C>T | upstream_gene_variant | 0.15 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.27 |
clpC1 | 4039452 | p.Pro418Gln | missense_variant | 0.25 |
embC | 4240581 | p.Leu240His | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243144 | c.-89C>A | upstream_gene_variant | 0.13 |
embA | 4243703 | c.471C>T | synonymous_variant | 0.14 |
embA | 4244223 | p.Ala331Pro | missense_variant | 0.29 |
embA | 4244934 | p.Thr568Pro | missense_variant | 0.18 |
embA | 4245083 | c.1851A>G | synonymous_variant | 0.18 |
embA | 4245095 | c.1863C>A | synonymous_variant | 0.17 |
embA | 4246020 | p.Ala930Ser | missense_variant | 0.2 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.21 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.5 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.58 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.58 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.18 |
embB | 4247472 | p.Phe320Tyr | missense_variant | 0.18 |
embB | 4247805 | p.Ala431Val | missense_variant | 0.13 |
embB | 4249083 | p.Thr857Lys | missense_variant | 0.15 |
embB | 4249186 | c.2673G>T | synonymous_variant | 0.12 |
aftB | 4267900 | p.Ala313Ser | missense_variant | 0.33 |
aftB | 4268478 | p.Ala120Val | missense_variant | 0.12 |
aftB | 4268776 | p.Ser21Gly | missense_variant | 0.18 |
aftB | 4268906 | c.-70C>A | upstream_gene_variant | 0.14 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.17 |
aftB | 4269771 | c.-935C>T | upstream_gene_variant | 0.15 |
ethR | 4328169 | p.Trp207Cys | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |