Run ID: ERR2229691
Sample name:
Date: 31-03-2023 17:27:29
Number of reads: 1164367
Percentage reads mapped: 99.21
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7517 | c.216G>A | synonymous_variant | 0.11 |
gyrA | 9542 | c.2244delA | frameshift_variant | 0.14 |
fgd1 | 491389 | p.Tyr203Asn | missense_variant | 0.14 |
mshA | 576471 | p.Gly375Val | missense_variant | 0.17 |
rpoB | 759788 | c.-19A>G | upstream_gene_variant | 0.12 |
rpoB | 759959 | c.153G>A | synonymous_variant | 0.29 |
rpoC | 765366 | p.Thr666Ile | missense_variant | 0.22 |
rpoC | 765965 | p.Arg866Ser | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776473 | p.Gln670Lys | missense_variant | 0.13 |
mmpL5 | 777196 | p.Glu429Gln | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801120 | p.Glu104Asp | missense_variant | 0.13 |
fbiC | 1303030 | c.100C>A | synonymous_variant | 0.12 |
fbiC | 1303496 | p.Pro189Gln | missense_variant | 0.12 |
fbiC | 1303702 | p.Gly258Ser | missense_variant | 0.4 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1303879 | p.Thr317Ser | missense_variant | 0.13 |
fbiC | 1304417 | p.Leu496His | missense_variant | 0.12 |
fbiC | 1304658 | c.1728C>T | synonymous_variant | 0.11 |
Rv1258c | 1406341 | p.Tyr334His | missense_variant | 0.15 |
Rv1258c | 1406348 | c.993C>T | synonymous_variant | 0.15 |
atpE | 1461014 | c.-31G>A | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.13 |
fabG1 | 1674143 | p.Ala235Val | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103173 | c.-131C>G | upstream_gene_variant | 0.17 |
ndh | 2103178 | c.-136G>T | upstream_gene_variant | 0.17 |
katG | 2154206 | p.Ala636Thr | missense_variant | 0.15 |
katG | 2154294 | c.1818C>A | synonymous_variant | 0.15 |
katG | 2154988 | p.Pro375Leu | missense_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169605 | c.1008T>C | synonymous_variant | 0.18 |
PPE35 | 2169618 | p.Phe332Ser | missense_variant | 0.1 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.77 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.77 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289972 | c.-731T>C | upstream_gene_variant | 0.12 |
eis | 2714221 | p.Ala371Gly | missense_variant | 0.15 |
eis | 2714629 | p.Leu235Pro | missense_variant | 0.18 |
eis | 2714688 | p.Phe215Leu | missense_variant | 0.67 |
eis | 2715074 | p.Val87Leu | missense_variant | 0.15 |
folC | 2746191 | p.Gly470Ser | missense_variant | 0.18 |
folC | 2746833 | p.Val256Met | missense_variant | 0.12 |
folC | 2747490 | p.Arg37Ser | missense_variant | 0.11 |
pepQ | 2859925 | p.Pro165Leu | missense_variant | 0.12 |
Rv2752c | 3064758 | c.1434G>A | synonymous_variant | 0.14 |
Rv2752c | 3065671 | p.Asp174Val | missense_variant | 0.17 |
Rv2752c | 3067049 | c.-858G>A | upstream_gene_variant | 0.11 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.27 |
fbiD | 3339012 | c.-106A>G | upstream_gene_variant | 0.1 |
fprA | 3473975 | c.-32G>A | upstream_gene_variant | 0.13 |
fprA | 3474368 | p.Gly121Ala | missense_variant | 0.12 |
fprA | 3475374 | c.1368C>A | synonymous_variant | 0.15 |
Rv3236c | 3612564 | p.Met185Leu | missense_variant | 0.11 |
alr | 3840761 | c.660G>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244794 | p.Val521Glu | missense_variant | 0.33 |
embB | 4245884 | c.-630C>T | upstream_gene_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.28 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.52 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4247090 | p.Thr193Ala | missense_variant | 0.14 |
aftB | 4267030 | p.Asp603Asn | missense_variant | 0.17 |
aftB | 4267054 | p.Tyr595His | missense_variant | 0.18 |
aftB | 4269255 | c.-419C>T | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |