Run ID: ERR2229601
Sample name:
Date: 31-03-2023 17:20:59
Number of reads: 1085773
Percentage reads mapped: 99.24
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 | 0.97 |
fgd1 | 491339 | p.Gly186Val | missense_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.27 |
mshA | 576687 | p.Glu447Gly | missense_variant | 0.11 |
ccsA | 619940 | p.Ala17Val | missense_variant | 0.14 |
rpoC | 764341 | c.972G>T | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776062 | p.Thr807Ser | missense_variant | 0.17 |
mmpL5 | 776150 | p.Met777Ile | missense_variant | 0.14 |
mmpL5 | 776173 | p.Asp770Asn | missense_variant | 0.12 |
mmpL5 | 777781 | p.Thr234Ala | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303564 | p.Gly212Ser | missense_variant | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304337 | c.1407C>A | synonymous_variant | 0.11 |
atpE | 1460852 | c.-192delT | upstream_gene_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674759 | c.558G>A | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154047 | p.Trp689Arg | missense_variant | 0.18 |
katG | 2154947 | p.Ile389Val | missense_variant | 0.13 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.28 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.28 |
PPE35 | 2167973 | c.2640A>G | synonymous_variant | 0.2 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.22 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.19 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.43 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.45 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289721 | c.-480C>A | upstream_gene_variant | 0.12 |
folC | 2746552 | c.1047C>T | synonymous_variant | 0.13 |
Rv2752c | 3065425 | p.Gly256Asp | missense_variant | 0.25 |
thyX | 3067444 | p.Arg168Cys | missense_variant | 0.15 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3474860 | p.Glu285Val | missense_variant | 0.15 |
Rv3236c | 3612080 | p.Ala346Asp | missense_variant | 0.13 |
fbiB | 3641931 | p.Arg133Ser | missense_variant | 0.15 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.28 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.15 |
clpC1 | 4039486 | p.Gly407Cys | missense_variant | 0.12 |
clpC1 | 4039546 | p.Asp387Asn | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243250 | c.18T>C | synonymous_variant | 0.11 |
embA | 4245586 | p.Pro785Leu | missense_variant | 0.14 |
embB | 4246034 | c.-480G>T | upstream_gene_variant | 0.12 |
ubiA | 4269137 | p.Tyr233His | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |