Run ID: SRR4035836
Sample name:
Date: 04-04-2023 07:19:46
Number of reads: 947804
Percentage reads mapped: 99.5
Strain: lineage4.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 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 | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491789 | p.Gly336Asp | missense_variant | 0.11 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 764263 | c.894G>A | synonymous_variant | 0.92 |
rpoC | 764364 | p.Gly332Asp | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776567 | p.Met638Ile | missense_variant | 0.11 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpL5 | 777347 | c.1134C>T | synonymous_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781568 | c.9C>T | synonymous_variant | 0.17 |
rplC | 801133 | p.Gly109Ser | missense_variant | 0.2 |
fbiC | 1304230 | p.Pro434Ser | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475423 | n.1766T>A | non_coding_transcript_exon_variant | 0.11 |
inhA | 1674498 | c.297G>A | synonymous_variant | 0.12 |
rpsA | 1833924 | p.Gly128Asp | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168041 | p.Ala858Thr | missense_variant | 0.18 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.27 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288807 | c.435C>T | synonymous_variant | 0.11 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518956 | p.Ala281Val | missense_variant | 0.12 |
folC | 2747002 | c.597T>C | synonymous_variant | 0.11 |
folC | 2747656 | c.-58G>T | upstream_gene_variant | 0.14 |
pepQ | 2859601 | c.817delG | frameshift_variant | 0.13 |
Rv2752c | 3066200 | c.-10delT | upstream_gene_variant | 0.13 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
clpC1 | 4038430 | c.2275C>T | synonymous_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4248942 | p.Gly810Asp | missense_variant | 0.12 |
embB | 4249731 | p.Ala1073Val | missense_variant | 0.13 |
aftB | 4267750 | p.Phe363Leu | missense_variant | 0.12 |
ubiA | 4269631 | p.Ala68Val | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407555 | c.648A>G | synonymous_variant | 0.12 |