Run ID: ERR2229340
Sample name:
Date: 31-03-2023 17:02:30
Number of reads: 1176906
Percentage reads mapped: 98.85
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 |
rpoB | 760769 | c.963C>A | synonymous_variant | 0.18 |
rpoB | 760790 | c.984C>A | synonymous_variant | 0.13 |
rpoB | 760954 | p.Ile383Thr | missense_variant | 0.11 |
rpoB | 761465 | c.1659G>A | synonymous_variant | 0.12 |
rpoC | 764148 | p.Ser260* | stop_gained | 0.12 |
rpoC | 764176 | p.Asp269Glu | missense_variant | 0.14 |
rpoC | 764630 | p.Arg421Ser | missense_variant | 0.17 |
rpoC | 765416 | p.Phe683Leu | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777000 | p.His494Leu | missense_variant | 0.2 |
mmpL5 | 777266 | c.1215G>T | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304848 | p.Asn640Asp | missense_variant | 0.1 |
fbiC | 1304969 | p.Leu680Pro | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473901 | n.244G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.13 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.13 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.37 |
inhA | 1674349 | p.Ile50Val | missense_variant | 0.11 |
inhA | 1674353 | p.Thr51Ile | missense_variant | 0.11 |
inhA | 1674568 | p.Ser123Pro | missense_variant | 0.12 |
rpsA | 1834937 | p.Ser466Cys | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102111 | p.Ile311Thr | missense_variant | 0.11 |
ndh | 2103011 | p.Pro11Gln | missense_variant | 0.13 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.15 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 0.19 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.17 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.16 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.41 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.39 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290146 | c.-905G>T | upstream_gene_variant | 0.15 |
kasA | 2519264 | p.Val384Ile | missense_variant | 0.15 |
folC | 2746654 | c.945C>T | synonymous_variant | 0.17 |
Rv2752c | 3064532 | p.Thr554Ala | missense_variant | 0.14 |
fbiD | 3339702 | c.585G>C | synonymous_variant | 0.12 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fbiB | 3642596 | c.1062C>A | synonymous_variant | 0.12 |
alr | 3841041 | p.Asp127Gly | missense_variant | 0.11 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.25 |
rpoA | 3877869 | p.Lys213Asn | missense_variant | 0.14 |
rpoA | 3878481 | c.26dupT | frameshift_variant | 0.15 |
rpoA | 3878487 | c.21C>A | synonymous_variant | 0.15 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.4 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.4 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.47 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.58 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.6 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.58 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.38 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.43 |
embB | 4247024 | p.Pro171Ala | missense_variant | 0.18 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.18 |
aftB | 4268691 | p.Phe49Tyr | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407664 | p.Ala180Glu | missense_variant | 0.13 |