Run ID: ERR2229674
Sample name:
Date: 31-03-2023 17:24:41
Number of reads: 549445
Percentage reads mapped: 99.19
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
ethA | 4327292 | p.Thr61Met | missense_variant | 0.22 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.11 |
fgd1 | 491071 | p.Tyr97Asn | missense_variant | 0.17 |
fgd1 | 491501 | p.Glu240Gly | missense_variant | 0.12 |
fgd1 | 491521 | c.739C>A | synonymous_variant | 0.12 |
fgd1 | 491574 | p.Asp264Glu | missense_variant | 0.12 |
rpoB | 759611 | c.-196G>T | upstream_gene_variant | 0.4 |
rpoC | 764210 | p.Ile281Val | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776307 | p.Asp725Gly | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407020 | c.321C>A | synonymous_variant | 0.12 |
embR | 1417090 | c.258C>T | synonymous_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102818 | c.225G>A | synonymous_variant | 0.4 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.4 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.4 |
PPE35 | 2168621 | c.1992C>T | synonymous_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169091 | p.Val508Leu | missense_variant | 0.33 |
PPE35 | 2169095 | p.Leu506Phe | missense_variant | 0.25 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519337 | p.Asn408Ile | missense_variant | 0.17 |
pepQ | 2860579 | c.-161A>C | upstream_gene_variant | 0.17 |
ald | 3087158 | c.339G>A | synonymous_variant | 0.15 |
ald | 3087195 | p.Ala126Thr | missense_variant | 0.12 |
ald | 3087872 | c.1053G>T | synonymous_variant | 0.12 |
whiB7 | 3568505 | c.175C>A | synonymous_variant | 0.15 |
alr | 3840504 | p.Asn306Ile | missense_variant | 0.29 |
rpoA | 3878622 | c.-115C>A | upstream_gene_variant | 1.0 |
clpC1 | 4040605 | p.Leu34Val | missense_variant | 0.14 |
panD | 4044003 | p.Met93Ile | missense_variant | 0.25 |
panD | 4044083 | p.Gly67Cys | missense_variant | 0.29 |
panD | 4044313 | c.-32C>T | upstream_gene_variant | 0.22 |
panD | 4044438 | c.-157G>T | upstream_gene_variant | 0.15 |
embC | 4239837 | c.-26A>G | upstream_gene_variant | 0.13 |
embC | 4241811 | p.Trp650Leu | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.19 |
embB | 4248833 | p.Trp774Gly | missense_variant | 0.2 |
ubiA | 4269777 | p.Lys19Asn | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407552 | c.651G>T | synonymous_variant | 0.17 |
gid | 4407626 | p.Ala193Ser | missense_variant | 0.17 |
gid | 4407891 | p.Met104Ile | missense_variant | 0.47 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |