Run ID: ERR2229744
Sample name:
Date: 31-03-2023 17:33:13
Number of reads: 1193536
Percentage reads mapped: 99.2
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 |
fgd1 | 491042 | p.Ala87Asp | missense_variant | 0.14 |
fgd1 | 491182 | p.Glu134* | stop_gained | 0.14 |
rpoB | 760409 | p.Ser201Arg | missense_variant | 0.17 |
rpoB | 760590 | p.Val262Ile | missense_variant | 0.11 |
rpoB | 762825 | p.Gly1007Arg | missense_variant | 0.14 |
rpoC | 765060 | p.Asn564Ile | missense_variant | 0.12 |
rpoC | 765682 | p.Asn771Lys | missense_variant | 0.15 |
rpoC | 766975 | c.3606C>A | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776745 | p.Arg579His | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304005 | p.Pro359Thr | missense_variant | 0.22 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.1 |
atpE | 1461008 | c.-37G>C | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474742 | n.1085A>G | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.28 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.28 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.26 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.26 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.26 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.41 |
rpsA | 1833392 | c.-150C>A | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155235 | p.Leu293Met | missense_variant | 0.22 |
katG | 2155998 | p.Trp38Cys | missense_variant | 0.12 |
PPE35 | 2167965 | c.2646_2647delAG | frameshift_variant | 0.12 |
PPE35 | 2167973 | c.2640A>G | synonymous_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.17 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.17 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.19 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.19 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.33 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.35 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.21 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747422 | c.177G>T | synonymous_variant | 0.12 |
pepQ | 2859418 | p.Gly334Asp | missense_variant | 0.12 |
fprA | 3474908 | p.Arg301Pro | missense_variant | 0.17 |
fbiB | 3641632 | p.Val33Asp | missense_variant | 0.11 |
fbiB | 3642768 | p.Leu412Met | missense_variant | 0.12 |
rpoA | 3877863 | c.645G>T | synonymous_variant | 0.14 |
rpoA | 3878636 | c.-129C>G | upstream_gene_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244278 | p.Pro349Gln | missense_variant | 0.12 |
embA | 4244930 | c.1698G>C | synonymous_variant | 0.2 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.44 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.53 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.4 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.4 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.28 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.28 |
embB | 4246832 | p.Lys107* | stop_gained | 0.17 |
embB | 4247036 | p.Gly175Cys | missense_variant | 0.12 |
embB | 4247090 | p.Thr193Ala | missense_variant | 0.15 |
embB | 4247098 | c.585C>G | synonymous_variant | 0.14 |
embB | 4247903 | c.1390C>A | synonymous_variant | 0.11 |
aftB | 4267786 | p.Gly351Trp | missense_variant | 0.17 |
aftB | 4268522 | p.Leu105Phe | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |