Run ID: ERR2229175
Sample name:
Date: 31-03-2023 16:46:58
Number of reads: 511817
Percentage reads mapped: 99.36
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
ethA | 4327113 | p.Gln121* | stop_gained | 0.22 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9131 | p.Gln610His | missense_variant | 0.22 |
gyrA | 9403 | p.Gln701Arg | missense_variant | 0.14 |
gyrA | 9496 | p.Ala732Val | missense_variant | 0.15 |
mshA | 575457 | p.Asn37Ile | missense_variant | 0.29 |
ccsA | 619956 | c.66G>A | synonymous_variant | 0.29 |
rpoB | 761156 | c.1350G>A | synonymous_variant | 0.22 |
rpoC | 765637 | c.2268C>A | synonymous_variant | 0.25 |
rpoC | 766294 | c.2925C>T | synonymous_variant | 0.14 |
rpoC | 766891 | c.3527delT | frameshift_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777001 | p.His494Asn | missense_variant | 0.12 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.2 |
mmpL5 | 777173 | c.1308C>T | synonymous_variant | 0.18 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.18 |
mmpR5 | 778451 | c.-539C>A | upstream_gene_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1303804 | p.Val292Met | missense_variant | 0.29 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.14 |
Rv1258c | 1406310 | p.Leu344Gln | missense_variant | 0.2 |
embR | 1417539 | c.-192G>T | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473553 | n.-105G>T | upstream_gene_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475838 | n.2181T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476522 | n.2865G>A | non_coding_transcript_exon_variant | 0.25 |
rpsA | 1834879 | p.Asp446Glu | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918060 | p.Lys41Glu | missense_variant | 0.25 |
tlyA | 1918456 | p.Arg173Ser | missense_variant | 0.15 |
ndh | 2102875 | c.168C>T | synonymous_variant | 0.22 |
katG | 2154578 | p.Gly512Arg | missense_variant | 0.12 |
katG | 2155182 | p.Lys310Asn | missense_variant | 0.18 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.18 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.21 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.22 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.22 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.24 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.4 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.44 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518348 | c.234A>T | synonymous_variant | 0.13 |
ahpC | 2725941 | c.-252C>T | upstream_gene_variant | 0.25 |
pepQ | 2859365 | p.Pro352Ser | missense_variant | 0.22 |
ribD | 2986869 | p.Asp11Asn | missense_variant | 0.15 |
Rv2752c | 3064633 | p.Ala520Val | missense_variant | 0.25 |
Rv2752c | 3065497 | p.Arg232Leu | missense_variant | 0.2 |
thyA | 3073815 | p.Gln219His | missense_variant | 0.17 |
thyA | 3074325 | c.147A>G | synonymous_variant | 0.22 |
fbiD | 3339136 | p.Asp7His | missense_variant | 0.12 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
alr | 3840211 | p.Glu404Lys | missense_variant | 0.2 |
clpC1 | 4038590 | c.2114delT | frameshift_variant | 0.2 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.2 |
clpC1 | 4039530 | p.Asp392Ala | missense_variant | 0.2 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.33 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.4 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.4 |
embB | 4248115 | c.1602C>T | synonymous_variant | 0.14 |
embB | 4249462 | c.2949G>T | synonymous_variant | 0.22 |
aftB | 4269213 | c.-377C>A | upstream_gene_variant | 0.29 |
ubiA | 4269239 | p.Ala199Thr | missense_variant | 0.33 |
ethA | 4327590 | c.-117G>T | upstream_gene_variant | 0.12 |
ethA | 4327774 | c.-301G>A | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |