Run ID: ERR2229091
Sample name:
Date: 31-03-2023 16:37:50
Number of reads: 369044
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 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 779650 | c.-745A>G | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305224 | p.Asp765Val | missense_variant | 0.15 |
embR | 1417178 | p.Thr57Asn | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474748 | n.1091T>A | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673251 | c.-189T>A | upstream_gene_variant | 0.2 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.25 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.25 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.43 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.43 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.43 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.5 |
rpsA | 1834953 | p.Ala471Val | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918729 | p.Ile264Phe | missense_variant | 0.22 |
katG | 2154374 | p.Asp580His | missense_variant | 0.25 |
katG | 2156177 | c.-66T>C | upstream_gene_variant | 0.14 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.33 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.33 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.33 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169023 | c.1590G>T | synonymous_variant | 0.25 |
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 | 0.2 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.22 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.2 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.22 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.26 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.25 |
PPE35 | 2169939 | p.Gly225Ala | missense_variant | 0.14 |
PPE35 | 2169941 | c.672C>T | synonymous_variant | 0.14 |
PPE35 | 2169944 | c.669G>C | synonymous_variant | 0.14 |
PPE35 | 2169947 | c.666T>C | synonymous_variant | 0.14 |
PPE35 | 2169956 | c.657T>C | synonymous_variant | 0.11 |
PPE35 | 2169964 | p.Leu217Val | missense_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.19 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.2 |
PPE35 | 2170232 | c.381T>C | synonymous_variant | 0.12 |
PPE35 | 2170235 | c.378T>C | synonymous_variant | 0.12 |
PPE35 | 2170238 | c.375T>G | synonymous_variant | 0.12 |
Rv1979c | 2222656 | p.Lys170Met | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517922 | c.-193C>T | upstream_gene_variant | 0.29 |
kasA | 2518360 | p.Tyr82* | stop_gained | 0.2 |
ahpC | 2726148 | c.-45A>T | upstream_gene_variant | 0.25 |
pepQ | 2859607 | p.Arg271Gln | missense_variant | 0.2 |
ribD | 2986934 | p.Tyr32* | stop_gained | 0.2 |
ald | 3087182 | p.Gln121His | missense_variant | 0.14 |
fbiA | 3641368 | p.Tyr276His | missense_variant | 0.2 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.18 |
rpoA | 3877996 | p.Val171Ala | missense_variant | 0.33 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.22 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.22 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.17 |
clpC1 | 4040320 | p.Ala129Thr | missense_variant | 0.2 |
embC | 4239921 | p.Arg20Leu | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247198 | p.Thr229Ser | missense_variant | 0.25 |
embB | 4249219 | p.Tyr902* | stop_gained | 0.4 |
aftB | 4269132 | c.-296G>A | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338678 | c.-157G>T | upstream_gene_variant | 0.14 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |