Run ID: ERR2229388
Sample name:
Date: 31-03-2023 17:08:57
Number of reads: 580886
Percentage reads mapped: 98.86
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5942 | p.Glu235Lys | missense_variant | 0.5 |
gyrB | 6049 | c.810G>C | synonymous_variant | 0.67 |
gyrA | 7054 | c.-248C>T | upstream_gene_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8534 | c.1233G>T | synonymous_variant | 0.13 |
fgd1 | 491084 | p.Val101Gly | missense_variant | 0.22 |
mshA | 576673 | c.1326G>A | synonymous_variant | 0.22 |
ccsA | 620099 | p.Arg70Pro | missense_variant | 0.67 |
rpoB | 761148 | p.Arg448* | stop_gained | 0.14 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.15 |
rpoB | 761947 | p.Leu714Gln | missense_variant | 0.22 |
rpoC | 764856 | p.Val496Ala | missense_variant | 0.15 |
rpoC | 765761 | p.Pro798Thr | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775700 | c.2781G>A | synonymous_variant | 0.33 |
mmpL5 | 775703 | c.2778A>G | synonymous_variant | 0.33 |
mmpL5 | 775715 | c.2766G>A | synonymous_variant | 0.29 |
mmpL5 | 775718 | c.2763C>G | synonymous_variant | 0.29 |
mmpL5 | 775726 | c.2755C>T | synonymous_variant | 0.25 |
mmpL5 | 775727 | c.2754C>G | synonymous_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800902 | p.Gly32Trp | missense_variant | 0.22 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473719 | n.62G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473940 | n.283A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.17 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.15 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.15 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.42 |
rpsA | 1833558 | p.Val6Asp | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918210 | p.Ala91Thr | missense_variant | 0.2 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.17 |
katG | 2154388 | p.Ser575Leu | missense_variant | 0.18 |
katG | 2156048 | p.Val22Phe | missense_variant | 0.14 |
katG | 2156361 | c.-250G>A | upstream_gene_variant | 0.29 |
PPE35 | 2167715 | p.Leu966Phe | missense_variant | 0.14 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.14 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.13 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.18 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.18 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.22 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169192 | p.Ala474Glu | missense_variant | 0.2 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.12 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.78 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.83 |
PPE35 | 2170345 | p.Ala90Ser | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518537 | c.423C>T | synonymous_variant | 0.33 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.33 |
eis | 2714150 | p.Pro395Thr | missense_variant | 0.12 |
folC | 2747452 | c.147G>T | synonymous_variant | 0.29 |
Rv2752c | 3065422 | p.Arg257Gln | missense_variant | 0.18 |
ald | 3087135 | p.Ala106Ser | missense_variant | 0.18 |
ald | 3087611 | c.792G>A | synonymous_variant | 0.2 |
fbiA | 3640377 | c.-166G>T | upstream_gene_variant | 0.2 |
fbiA | 3640811 | p.Gln90Arg | missense_variant | 0.22 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.23 |
alr | 3841582 | c.-162A>G | upstream_gene_variant | 0.14 |
alr | 3841584 | c.-164C>A | upstream_gene_variant | 0.14 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.19 |
rpoA | 3877826 | p.Glu228Gln | missense_variant | 0.33 |
ddn | 3986960 | c.117C>A | synonymous_variant | 0.17 |
ddn | 3987252 | p.Gln137Lys | missense_variant | 0.15 |
clpC1 | 4040741 | c.-37G>A | upstream_gene_variant | 0.22 |
embC | 4239778 | c.-85C>A | upstream_gene_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245015 | p.Ile595Phe | missense_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.33 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.38 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.44 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.45 |
embB | 4246987 | p.Phe158Leu | missense_variant | 0.29 |
embB | 4249230 | p.Gly906Val | missense_variant | 0.14 |
aftB | 4268418 | p.Glu140Gly | missense_variant | 0.4 |
ubiA | 4269356 | p.Arg160Cys | missense_variant | 0.33 |
whiB6 | 4338341 | p.Leu61Met | missense_variant | 0.14 |
whiB6 | 4338349 | p.Arg58His | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338607 | c.-86C>T | upstream_gene_variant | 0.25 |