Run ID: SRR6831905
Sample name:
Date: 04-04-2023 17:06:31
Number of reads: 647953
Percentage reads mapped: 99.72
Strain: lineage4.3.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5214 | c.-26C>G | upstream_gene_variant | 1.0 |
gyrB | 6284 | p.Asp349Tyr | missense_variant | 0.25 |
gyrA | 6727 | c.-575G>A | upstream_gene_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8972 | c.1671C>T | synonymous_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576789 | c.1442G>T | stop_lost&splice_region_variant | 0.18 |
ccsA | 620371 | c.485delC | frameshift_variant | 0.18 |
rpoC | 763407 | p.Gly13Asp | missense_variant | 0.4 |
rpoC | 764434 | p.Lys355Asn | missense_variant | 0.13 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775887 | p.Gly865Ala | missense_variant | 0.2 |
mmpL5 | 777595 | p.Glu296Lys | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305482 | p.Tyr851Ser | missense_variant | 0.22 |
Rv1258c | 1406693 | c.648G>T | synonymous_variant | 0.1 |
atpE | 1461014 | c.-31G>A | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473513 | n.-145T>C | upstream_gene_variant | 0.14 |
rrl | 1475362 | n.1705G>T | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1833738 | p.Arg66His | missense_variant | 0.12 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154807 | c.1305C>A | synonymous_variant | 0.25 |
Rv1979c | 2222015 | p.Val384Ile | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
folC | 2747651 | c.-53C>T | upstream_gene_variant | 0.29 |
pepQ | 2860199 | p.Ala74Thr | missense_variant | 0.2 |
Rv2752c | 3064692 | p.Asp500Glu | missense_variant | 0.14 |
Rv2752c | 3067135 | c.-944C>T | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841421 | c.-1A>G | upstream_gene_variant | 0.18 |
rpoA | 3878427 | p.Glu27Asp | missense_variant | 0.14 |
ddn | 3987215 | c.372A>G | synonymous_variant | 0.12 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040858 | c.-154G>T | upstream_gene_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4246227 | c.2997delT | frameshift_variant | 0.15 |
embB | 4248334 | c.1821C>T | synonymous_variant | 0.2 |
embB | 4248520 | c.2007C>T | synonymous_variant | 0.12 |
aftB | 4267280 | c.1557G>A | synonymous_variant | 0.12 |
ethA | 4326069 | c.1405C>A | synonymous_variant | 0.29 |
ethR | 4327673 | p.Leu42Arg | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407720 | c.483C>G | synonymous_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |