Run ID: ERR2229657
Sample name:
Date: 31-03-2023 17:23:51
Number of reads: 909146
Percentage reads mapped: 99.4
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 |
---|---|---|---|---|
gyrB | 6035 | p.Arg266Ser | missense_variant | 0.12 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7777 | p.Arg159Leu | missense_variant | 0.11 |
ccsA | 620033 | p.Ala48Asp | missense_variant | 0.11 |
rpoB | 761296 | p.Tyr497Phe | missense_variant | 0.11 |
rpoC | 764059 | c.690G>A | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775834 | p.Ala883Ser | missense_variant | 0.12 |
mmpL5 | 778522 | c.-42A>G | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407413 | c.-73C>G | upstream_gene_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471776 | n.-70G>T | upstream_gene_variant | 0.12 |
rrs | 1473146 | n.1301G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474425 | n.768A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475499 | n.1842C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475789 | n.2132C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476114 | n.2457T>C | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.27 |
inhA | 1673574 | c.-628C>A | upstream_gene_variant | 0.12 |
rpsA | 1833544 | c.3G>A | start_lost | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154485 | p.Leu543Ile | missense_variant | 0.12 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.16 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.1 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.1 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.39 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.39 |
Rv1979c | 2222517 | c.648C>T | synonymous_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715116 | p.Gly73Ser | missense_variant | 0.12 |
Rv2752c | 3064904 | p.Asp430Tyr | missense_variant | 0.17 |
Rv2752c | 3065255 | p.Ser313Thr | missense_variant | 0.13 |
Rv2752c | 3065638 | p.Leu185Pro | missense_variant | 0.1 |
Rv3236c | 3612658 | c.459G>T | synonymous_variant | 0.18 |
alr | 3840825 | p.Tyr199Cys | missense_variant | 0.15 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.12 |
embC | 4242053 | p.Tyr731Asn | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326099 | p.Gln459* | stop_gained | 0.14 |
ethA | 4326110 | p.Trp455Leu | missense_variant | 0.15 |
ethA | 4327329 | p.Arg49Ser | missense_variant | 0.2 |
ethA | 4327442 | p.Gly11Asp | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408019 | p.Gly62Cys | missense_variant | 0.14 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |