Run ID: ERR2229798
Sample name:
Date: 31-03-2023 17:35:55
Number of reads: 455924
Percentage reads mapped: 99.64
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 |
rpoC | 763619 | p.Arg84Cys | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775741 | c.2740C>T | synonymous_variant | 0.17 |
mmpL5 | 775747 | p.Met912Leu | missense_variant | 0.18 |
mmpL5 | 775748 | c.2733T>C | synonymous_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475200 | n.1543T>A | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833881 | p.Gly114Ser | missense_variant | 0.29 |
rpsA | 1833887 | p.Ile116Val | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918670 | p.Arg244His | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169192 | p.Ala474Glu | missense_variant | 0.12 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.17 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.17 |
PPE35 | 2169518 | c.1094delG | frameshift_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289525 | c.-284G>C | upstream_gene_variant | 0.17 |
thyA | 3074232 | p.Trp80Cys | missense_variant | 0.29 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
clpC1 | 4038637 | p.Tyr690His | missense_variant | 0.13 |
clpC1 | 4040410 | p.Gly99Cys | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.25 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.25 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.25 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.13 |
embB | 4247472 | p.Phe320Tyr | missense_variant | 0.13 |
embB | 4247691 | p.Thr393Asn | missense_variant | 0.11 |
aftB | 4267473 | p.Gly455Asp | missense_variant | 0.2 |
ubiA | 4269742 | p.Leu31Gln | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448508 | c.6_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |