Run ID: ERR775806
Sample name:
Date: 02-04-2023 05:43:13
Number of reads: 644946
Percentage reads mapped: 98.21
Strain: lineage4.4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | 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 | 8964 | p.Val555Ile | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575581 | c.234C>T | synonymous_variant | 0.13 |
rpoB | 762384 | p.Asn860Tyr | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.25 |
fbiC | 1304066 | p.Ala379Val | missense_variant | 0.18 |
Rv1258c | 1406348 | c.993C>A | synonymous_variant | 0.13 |
embR | 1416342 | p.Gly336Cys | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471778 | n.-68G>A | upstream_gene_variant | 1.0 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472479 | n.634C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473055 | n.1210C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715211 | p.Pro41Arg | missense_variant | 1.0 |
pepQ | 2859328 | p.Arg364Leu | missense_variant | 0.2 |
pepQ | 2860517 | c.-99C>A | upstream_gene_variant | 0.12 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 1.0 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
ethA | 4327068 | p.Leu136Met | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |