Run ID: SRR4034317
Sample name:
Date: 04-04-2023 06:42:47
Number of reads: 525011
Percentage reads mapped: 99.49
Strain: lineage4.1.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288896 | c.345delA | frameshift_variant | 0.22 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5184 | c.-56A>G | upstream_gene_variant | 0.2 |
gyrB | 6308 | p.Val357Leu | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7736 | c.435C>A | synonymous_variant | 0.29 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 8884 | p.Arg528His | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575519 | p.Ala58Thr | missense_variant | 0.14 |
mshA | 576628 | c.1281G>A | synonymous_variant | 0.2 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761487 | p.Glu561* | stop_gained | 0.14 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766778 | p.Glu1137* | stop_gained | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpL5 | 777933 | p.Lys183Arg | missense_variant | 0.2 |
mmpR5 | 778055 | c.-935G>A | upstream_gene_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781915 | p.Ala119Asp | missense_variant | 0.14 |
fbiC | 1303821 | c.892_893delAA | frameshift_variant | 0.2 |
fbiC | 1305288 | c.2358C>A | synonymous_variant | 0.29 |
Rv1258c | 1406185 | p.Pro386Ser | missense_variant | 0.2 |
Rv1258c | 1406691 | p.Arg217Leu | missense_variant | 0.2 |
Rv1258c | 1406744 | c.597G>A | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471775 | n.-71G>T | upstream_gene_variant | 0.22 |
rrl | 1474086 | n.429A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475441 | n.1785dupC | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475471 | n.1814C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476176 | n.2519C>A | non_coding_transcript_exon_variant | 0.33 |
inhA | 1673469 | c.-733A>G | upstream_gene_variant | 0.17 |
inhA | 1674332 | p.Leu44Pro | missense_variant | 0.11 |
rpsA | 1833987 | p.Pro149His | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102178 | p.Leu289Ile | missense_variant | 0.15 |
katG | 2154586 | p.Asp509Ala | missense_variant | 0.25 |
katG | 2155218 | p.Leu298Phe | missense_variant | 0.22 |
PPE35 | 2170100 | c.513G>T | synonymous_variant | 0.29 |
PPE35 | 2170699 | c.-87C>T | upstream_gene_variant | 0.13 |
Rv1979c | 2222096 | p.Ala357Ser | missense_variant | 0.25 |
Rv1979c | 2222967 | c.198G>T | synonymous_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518066 | c.-48delC | upstream_gene_variant | 0.2 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714956 | p.Tyr126Cys | missense_variant | 0.22 |
ahpC | 2726621 | p.Glu143Asp | missense_variant | 0.33 |
folC | 2746802 | p.Leu266Gln | missense_variant | 0.25 |
Rv2752c | 3064597 | p.Gly532Val | missense_variant | 0.14 |
thyX | 3067342 | p.Glu202* | stop_gained | 0.2 |
thyX | 3067919 | c.27G>T | synonymous_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087287 | c.468C>A | synonymous_variant | 0.22 |
Rv3083 | 3448317 | c.-187G>T | upstream_gene_variant | 0.22 |
fprA | 3473831 | c.-176G>T | upstream_gene_variant | 0.17 |
fprA | 3473976 | c.-31C>T | upstream_gene_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3612497 | p.Gly207Asp | missense_variant | 0.17 |
fbiB | 3641937 | p.Gly135Trp | missense_variant | 0.18 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.5 |
alr | 3840323 | c.1098C>T | synonymous_variant | 0.22 |
alr | 3841060 | p.Gly121Trp | missense_variant | 0.29 |
rpoA | 3878144 | c.363delC | frameshift_variant | 0.29 |
embC | 4242299 | p.Gly813Trp | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4246317 | p.Pro1029Thr | missense_variant | 0.15 |
embB | 4247323 | c.810G>T | synonymous_variant | 0.25 |
embB | 4247483 | p.Gly324Cys | missense_variant | 0.18 |
embB | 4248322 | c.1809G>A | synonymous_variant | 0.22 |
aftB | 4267164 | p.Trp558Leu | missense_variant | 0.2 |
ethA | 4328160 | c.-687C>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408029 | c.174C>A | synonymous_variant | 0.17 |