Run ID: SRR19392938
Sample name:
Date: 03-04-2023 21:37:06
Number of reads: 1557342
Percentage reads mapped: 99.64
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6233 | p.Ala332Thr | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491318 | p.Pro179Leu | missense_variant | 0.25 |
mshA | 575947 | c.600G>T | synonymous_variant | 0.2 |
mshA | 576542 | p.Ala399Ser | missense_variant | 0.25 |
rpoB | 761690 | c.1884G>T | synonymous_variant | 0.15 |
rpoB | 762712 | p.Pro969Leu | missense_variant | 0.14 |
rpoB | 762719 | p.Phe971Leu | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303701 | c.771C>T | synonymous_variant | 1.0 |
fbiC | 1304001 | c.1071C>A | synonymous_variant | 0.18 |
Rv1258c | 1407143 | c.198C>A | synonymous_variant | 0.17 |
Rv1258c | 1407522 | c.-182C>A | upstream_gene_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918098 | c.159C>T | synonymous_variant | 0.33 |
katG | 2155766 | p.His116Asn | missense_variant | 0.29 |
PPE35 | 2170067 | c.546C>T | synonymous_variant | 1.0 |
PPE35 | 2170312 | p.Arg101Trp | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518630 | c.516G>T | synonymous_variant | 0.22 |
folC | 2746497 | p.His368Asn | missense_variant | 0.14 |
pepQ | 2859596 | p.Ala275Ser | missense_variant | 0.18 |
ribD | 2987289 | p.Asp151Tyr | missense_variant | 0.25 |
ribD | 2987393 | c.555C>A | synonymous_variant | 0.15 |
thyX | 3067280 | c.666G>T | synonymous_variant | 0.5 |
thyX | 3067490 | c.456C>A | synonymous_variant | 0.5 |
ald | 3087305 | c.486G>T | synonymous_variant | 0.14 |
fbiD | 3339409 | p.Ala98Ser | missense_variant | 0.14 |
fbiD | 3339585 | c.468C>A | synonymous_variant | 1.0 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fbiB | 3641877 | c.343C>A | synonymous_variant | 0.13 |
fbiB | 3641991 | p.Gly153* | stop_gained | 0.5 |
fbiB | 3642024 | p.Ala164Ser | missense_variant | 0.33 |
fbiB | 3642211 | p.Gly226Val | missense_variant | 1.0 |
alr | 3840764 | c.657G>C | synonymous_variant | 1.0 |
clpC1 | 4038221 | c.2484C>A | synonymous_variant | 0.14 |
embC | 4240491 | p.Pro210Arg | missense_variant | 0.17 |
embC | 4241641 | p.Phe593Leu | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242677 | p.Thr939Ser | missense_variant | 0.13 |
embA | 4243487 | c.255C>T | synonymous_variant | 0.13 |
embA | 4244216 | c.984C>A | synonymous_variant | 0.25 |
embA | 4244678 | c.1446G>T | synonymous_variant | 0.17 |
embA | 4245487 | p.Pro752Gln | missense_variant | 0.18 |
embB | 4245554 | c.-960C>A | upstream_gene_variant | 0.2 |
embA | 4245557 | p.Glu775Asp | missense_variant | 0.2 |
embB | 4245662 | c.-852G>T | upstream_gene_variant | 0.17 |
embB | 4246774 | c.261G>A | synonymous_variant | 0.33 |
embB | 4247008 | p.Lys165Asn | missense_variant | 0.17 |
whiB6 | 4338208 | p.Pro105Gln | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |