Run ID: ERR11049033
Sample name:
Date: 31-03-2023 07:03:07
Number of reads: 501761
Percentage reads mapped: 99.61
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 |
gyrA | 9011 | c.1710C>T | synonymous_variant | 1.0 |
mshA | 576776 | p.Gly477Arg | missense_variant | 0.15 |
rpoB | 762110 | c.2304G>A | synonymous_variant | 0.12 |
rpoB | 762163 | p.Ile786Ser | missense_variant | 0.2 |
rpoB | 762594 | p.Leu930Met | missense_variant | 0.14 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.5 |
rpoC | 767229 | p.Ser1287Leu | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776207 | c.2274G>T | synonymous_variant | 0.11 |
mmpL5 | 776739 | p.Ile581Thr | missense_variant | 1.0 |
rpsL | 781383 | c.-177G>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781874 | p.Gln105His | missense_variant | 1.0 |
rplC | 800946 | c.138T>A | synonymous_variant | 0.14 |
fbiC | 1303155 | c.225G>C | synonymous_variant | 0.4 |
fbiC | 1304254 | p.Ala442Thr | missense_variant | 0.13 |
Rv1258c | 1406455 | p.Leu296Val | missense_variant | 0.15 |
Rv1258c | 1406995 | p.Phe116Val | missense_variant | 0.15 |
embR | 1416974 | p.Ala125Gly | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471800 | n.-45_-38delATTTCTAA | upstream_gene_variant | 1.0 |
rrs | 1472556 | n.711C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475511 | n.1854G>A | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673549 | p.Ala37Asp | missense_variant | 0.3 |
inhA | 1674830 | p.Glu210Val | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918151 | p.Val71Gly | missense_variant | 0.2 |
tlyA | 1918514 | p.Val192Gly | missense_variant | 0.22 |
ndh | 2102852 | c.190delT | frameshift_variant | 0.12 |
katG | 2154696 | c.1416A>G | synonymous_variant | 0.14 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2168222 | c.2390delC | frameshift_variant | 0.17 |
PPE35 | 2168307 | p.Phe769Ser | missense_variant | 0.22 |
PPE35 | 2168745 | p.Gly623Asp | missense_variant | 1.0 |
Rv1979c | 2222826 | p.Phe113Leu | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288923 | p.Glu107Lys | missense_variant | 0.18 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.67 |
folC | 2746584 | p.Leu339Val | missense_variant | 0.25 |
folC | 2747226 | p.Arg125Gly | missense_variant | 0.13 |
pepQ | 2860203 | p.Glu72Asp | missense_variant | 0.2 |
ribD | 2986868 | c.30T>A | synonymous_variant | 0.13 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.6 |
Rv2752c | 3065028 | c.1164G>A | synonymous_variant | 0.18 |
thyX | 3067320 | p.Arg209Gln | missense_variant | 0.33 |
fbiD | 3339053 | c.-65G>C | upstream_gene_variant | 0.2 |
fbiA | 3640882 | p.Val114Met | missense_variant | 0.12 |
fbiB | 3642432 | c.898C>T | synonymous_variant | 0.12 |
alr | 3841566 | c.-146C>T | upstream_gene_variant | 0.12 |
clpC1 | 4038725 | c.1980C>T | synonymous_variant | 0.15 |
clpC1 | 4040550 | p.Leu52Trp | missense_variant | 0.15 |
panD | 4044367 | c.-86A>T | upstream_gene_variant | 0.11 |
embC | 4241007 | p.Ala382Val | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4246302 | p.Ser1024Arg | missense_variant | 0.14 |
embB | 4247145 | p.Ser211Phe | missense_variant | 1.0 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.3 |
embB | 4249268 | p.Asp919Asn | missense_variant | 0.12 |
embB | 4249354 | c.2841G>C | synonymous_variant | 1.0 |
aftB | 4267153 | p.Ala562Pro | missense_variant | 0.22 |
aftB | 4267165 | p.Trp558Gly | missense_variant | 0.22 |
aftB | 4268952 | c.-116G>C | upstream_gene_variant | 0.17 |
whiB6 | 4338200 | p.Asp108His | missense_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407720 | c.483C>T | synonymous_variant | 0.17 |
gid | 4408096 | p.Val36Gly | missense_variant | 0.4 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |