Run ID: SRR13837447
Sample name:
Date: 03-04-2023 09:10:37
Number of reads: 881500
Percentage reads mapped: 98.01
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
ccsA | 620144 | c.255dupT | frameshift_variant | 1.0 |
rpoB | 760191 | p.Val129Phe | missense_variant | 1.0 |
rpoB | 760311 | p.Val169Leu | missense_variant | 1.0 |
rpoB | 762805 | p.Gly1000Asp | missense_variant | 1.0 |
rpoB | 762963 | p.Gly1053Arg | missense_variant | 1.0 |
rpoC | 763662 | p.Ala98Asp | missense_variant | 1.0 |
mmpL5 | 776041 | p.Ala814Thr | missense_variant | 1.0 |
mmpL5 | 776070 | c.2410delA | frameshift_variant | 1.0 |
mmpL5 | 777800 | c.681C>T | synonymous_variant | 1.0 |
fbiC | 1304996 | p.Leu689Ser | missense_variant | 1.0 |
Rv1258c | 1407148 | p.Ala65Ser | missense_variant | 1.0 |
embR | 1416842 | p.Asp169Gly | missense_variant | 1.0 |
inhA | 1674940 | c.739_740insG | frameshift_variant | 1.0 |
ndh | 2102694 | p.Val117Ile | missense_variant | 1.0 |
katG | 2155865 | p.Val83Met | missense_variant | 1.0 |
PPE35 | 2168123 | c.2489dupG | frameshift_variant | 1.0 |
PPE35 | 2170268 | c.345C>A | synonymous_variant | 1.0 |
kasA | 2518311 | p.Asp66Gly | missense_variant | 1.0 |
eis | 2714666 | p.Tyr223Asp | missense_variant | 1.0 |
ahpC | 2726589 | p.Arg133Ser | missense_variant | 1.0 |
Rv2752c | 3066289 | c.-98T>G | upstream_gene_variant | 1.0 |
thyA | 3074418 | p.Lys18Asn | missense_variant | 1.0 |
ald | 3087163 | c.344_345insC | frameshift_variant | 1.0 |
Rv3236c | 3612049 | c.1068G>C | synonymous_variant | 1.0 |
Rv3236c | 3612400 | c.717G>A | synonymous_variant | 1.0 |
fbiB | 3642445 | p.Ala304Gly | missense_variant | 1.0 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
clpC1 | 4040104 | p.Met201Leu | missense_variant | 1.0 |
embC | 4241480 | c.1618T>C | synonymous_variant | 1.0 |
embB | 4249483 | c.2970C>G | synonymous_variant | 1.0 |
aftB | 4268164 | c.672_673insA | frameshift_variant | 1.0 |
ethA | 4327641 | c.-168G>A | upstream_gene_variant | 1.0 |