Run ID: ERR2229335
Sample name:
Date: 31-03-2023 17:03:29
Number of reads: 1358064
Percentage reads mapped: 98.9
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 |
---|---|---|---|---|
gyrB | 6001 | c.762G>T | synonymous_variant | 0.19 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.32 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.14 |
mshA | 576532 | c.1185C>T | synonymous_variant | 0.13 |
ccsA | 620592 | c.702C>A | synonymous_variant | 0.12 |
rpoB | 760437 | p.Asp211Asn | missense_variant | 0.22 |
rpoB | 760445 | c.639C>A | synonymous_variant | 0.29 |
rpoB | 762531 | c.2727delT | frameshift_variant | 0.14 |
rpoC | 764535 | p.Arg389Pro | missense_variant | 0.21 |
rpoC | 766822 | c.3453C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776049 | p.Ser811* | stop_gained | 0.18 |
mmpR5 | 778139 | c.-851G>A | upstream_gene_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304043 | p.Trp371Cys | missense_variant | 0.15 |
Rv1258c | 1406943 | c.397_398insGC | frameshift_variant | 0.14 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.14 |
Rv1258c | 1406948 | c.391_392delGC | frameshift_variant | 0.14 |
embR | 1416916 | c.432A>G | synonymous_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 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.15 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.12 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.12 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.39 |
inhA | 1674770 | p.Ala190Asp | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102074 | p.Met323Lys | missense_variant | 0.23 |
ndh | 2102202 | p.Ser281Ala | missense_variant | 0.15 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.13 |
katG | 2155139 | p.Pro325Thr | missense_variant | 0.12 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.17 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.16 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.11 |
PPE35 | 2169447 | p.Phe389Ser | missense_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.6 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.62 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519346 | p.Leu411Pro | missense_variant | 0.12 |
Rv2752c | 3066187 | c.4delG | frameshift_variant | 0.14 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.19 |
thyX | 3067877 | c.69G>A | synonymous_variant | 0.13 |
thyA | 3074451 | c.21G>C | synonymous_variant | 0.22 |
fprA | 3474011 | p.Arg2His | missense_variant | 0.12 |
whiB7 | 3568534 | p.Arg49Met | missense_variant | 0.2 |
Rv3236c | 3612589 | c.528C>G | synonymous_variant | 0.2 |
fbiB | 3642796 | p.Leu421* | stop_gained | 0.15 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.2 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.13 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.12 |
clpC1 | 4040331 | p.Val125Gly | missense_variant | 0.17 |
embC | 4239835 | c.-28C>T | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244564 | c.1332G>T | synonymous_variant | 0.11 |
embA | 4245268 | p.Asn679Ser | missense_variant | 0.12 |
embA | 4245974 | p.Ile914Met | missense_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.21 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.42 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.5 |
aftB | 4267895 | p.Phe314Leu | missense_variant | 0.21 |
ubiA | 4269125 | p.Ala237Ser | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407858 | c.345G>T | synonymous_variant | 0.15 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |