Run ID: ERR2229307
Sample name:
Date: 31-03-2023 16:59:48
Number of reads: 1215713
Percentage reads mapped: 99.27
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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.16 |
rpoC | 763743 | p.Leu125Gln | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305006 | p.Glu692Asp | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473975 | n.318G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.11 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.23 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.22 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.24 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.35 |
inhA | 1674352 | p.Thr51Ser | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101857 | p.Trp396Gly | missense_variant | 0.12 |
ndh | 2102954 | p.Ala30Val | missense_variant | 0.14 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 0.11 |
PPE35 | 2168143 | p.Phe824Leu | missense_variant | 0.11 |
PPE35 | 2168150 | c.2463T>C | synonymous_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.47 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.45 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289074 | p.Asp56Glu | missense_variant | 0.13 |
pncA | 2289718 | c.-477G>T | upstream_gene_variant | 0.29 |
kasA | 2518704 | p.Gly197Asp | missense_variant | 0.14 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.29 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.29 |
ahpC | 2725938 | c.-255_-254insA | upstream_gene_variant | 0.12 |
pepQ | 2859845 | p.Thr192Pro | missense_variant | 0.22 |
ribD | 2986853 | c.15T>A | synonymous_variant | 0.12 |
thyA | 3074281 | p.Arg64Leu | missense_variant | 0.13 |
ald | 3087846 | p.Leu343Ile | missense_variant | 0.13 |
fprA | 3474052 | p.Phe16Val | missense_variant | 0.15 |
Rv3236c | 3612011 | p.Leu369Gln | missense_variant | 0.12 |
fbiB | 3642509 | c.975C>A | synonymous_variant | 0.25 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.19 |
rpoA | 3878599 | c.-92C>G | upstream_gene_variant | 1.0 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.17 |
embC | 4241561 | p.Arg567Cys | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244282 | c.1050C>A | synonymous_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.21 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.29 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.29 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.29 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.17 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.17 |
embB | 4249101 | p.Tyr863Cys | missense_variant | 0.12 |
aftB | 4267251 | p.Asp529Gly | missense_variant | 0.12 |
aftB | 4268921 | c.-85C>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |