Run ID: ERR2229485
Sample name:
Date: 31-03-2023 17:15:17
Number of reads: 1147399
Percentage reads mapped: 99.22
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 |
gyrA | 7593 | p.Arg98Ser | missense_variant | 0.12 |
fgd1 | 491105 | p.Gly108Val | missense_variant | 0.12 |
mshA | 575387 | p.Ala14Thr | missense_variant | 0.14 |
ccsA | 620209 | c.323delG | frameshift_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775813 | p.Phe890Val | missense_variant | 0.13 |
mmpL5 | 775817 | c.2664T>C | synonymous_variant | 0.14 |
mmpL5 | 775820 | c.2661G>A | synonymous_variant | 0.14 |
mmpL5 | 777482 | c.999G>A | synonymous_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305040 | p.Ser704Pro | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475484 | n.1827A>C | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.23 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155191 | c.921A>C | synonymous_variant | 0.12 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.11 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.47 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.47 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.12 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.19 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.18 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.48 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.47 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518641 | p.Glu176Gly | missense_variant | 0.12 |
kasA | 2518798 | c.684G>A | synonymous_variant | 0.17 |
kasA | 2518897 | c.783G>T | synonymous_variant | 0.2 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.14 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.14 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.14 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.14 |
eis | 2714271 | c.1062C>T | synonymous_variant | 0.12 |
ribD | 2987220 | p.Arg128Ser | missense_variant | 0.15 |
fbiD | 3339444 | p.Asn109Lys | missense_variant | 0.12 |
fbiD | 3339523 | c.406C>A | synonymous_variant | 0.13 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3475338 | c.1332G>A | synonymous_variant | 0.14 |
Rv3236c | 3613296 | c.-180T>G | upstream_gene_variant | 0.12 |
Rv3236c | 3613303 | c.-187C>A | upstream_gene_variant | 0.13 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.22 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.13 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242688 | c.-545G>A | upstream_gene_variant | 0.15 |
embA | 4244551 | p.Ala440Asp | missense_variant | 0.22 |
embA | 4244594 | c.1362G>A | synonymous_variant | 0.18 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.6 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.67 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.67 |
embB | 4246792 | c.279C>T | synonymous_variant | 0.14 |
aftB | 4268537 | c.300G>T | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |