Run ID: ERR2229188
Sample name:
Date: 31-03-2023 16:47:14
Number of reads: 980428
Percentage reads mapped: 99.2
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 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 |
mshA | 576005 | p.Glu220* | stop_gained | 0.13 |
mshA | 576591 | p.Arg415Leu | missense_variant | 0.18 |
rpoC | 765775 | c.2406C>T | synonymous_variant | 0.14 |
rpoC | 766860 | p.Arg1164Leu | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 778598 | p.Ile103Thr | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303580 | p.Thr217Met | missense_variant | 0.13 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304866 | p.Gly646Arg | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472469 | n.624G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.14 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.29 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169143 | c.1470G>T | synonymous_variant | 0.14 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.12 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.12 |
PPE35 | 2169748 | p.Ile289Phe | missense_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.39 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.41 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.15 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.14 |
folC | 2746244 | p.Ala452Asp | missense_variant | 0.2 |
folC | 2746411 | c.1188G>T | synonymous_variant | 0.12 |
folC | 2746879 | p.Lys240Asn | missense_variant | 0.17 |
Rv2752c | 3064666 | p.Arg509Pro | missense_variant | 0.11 |
Rv2752c | 3064850 | c.1341dupG | frameshift_variant | 0.15 |
Rv2752c | 3064855 | p.Lys446Arg | missense_variant | 0.17 |
Rv3236c | 3613194 | c.-78C>A | upstream_gene_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.16 |
clpC1 | 4038504 | p.Met734Lys | missense_variant | 0.16 |
embC | 4240801 | c.939C>T | synonymous_variant | 0.13 |
embC | 4240803 | p.Tyr314Phe | missense_variant | 0.14 |
embC | 4241660 | p.Leu600Met | missense_variant | 0.17 |
embA | 4242322 | c.-911C>T | upstream_gene_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243173 | c.-60A>G | upstream_gene_variant | 0.12 |
embA | 4244137 | p.Ala302Glu | missense_variant | 0.12 |
embA | 4245398 | p.Asn722Lys | missense_variant | 0.17 |
embB | 4246915 | c.402C>T | synonymous_variant | 0.13 |
aftB | 4268850 | c.-14T>C | upstream_gene_variant | 0.15 |
aftB | 4268873 | c.-37C>A | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |