Run ID: ERR4812871
Sample name:
Date: 01-04-2023 12:23:38
Number of reads: 637017
Percentage reads mapped: 99.27
Strain: lineage4
Drug-resistance: MDR-TB
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 |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289009 | p.Gly78Val | missense_variant | 0.17 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5787 | p.Thr183Met | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8379 | p.Gln360* | stop_gained | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490834 | p.Arg18Cys | missense_variant | 0.15 |
fgd1 | 490854 | c.72C>A | synonymous_variant | 0.17 |
fgd1 | 491115 | c.333G>T | synonymous_variant | 0.25 |
mshA | 576091 | c.744C>A | synonymous_variant | 0.2 |
mshA | 576123 | p.Leu259Arg | missense_variant | 0.29 |
rpoB | 761358 | p.Val518Ile | missense_variant | 0.17 |
rpoB | 762832 | p.Ser1009Ile | missense_variant | 0.18 |
rpoC | 762887 | c.-483G>T | upstream_gene_variant | 0.13 |
rpoC | 762944 | c.-426C>A | upstream_gene_variant | 0.14 |
rpoC | 764868 | p.Arg500His | missense_variant | 0.14 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406307 | p.Arg345His | missense_variant | 0.33 |
embR | 1416955 | p.Phe131Leu | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673431 | c.-771G>A | upstream_gene_variant | 1.0 |
inhA | 1674838 | p.Ala213Thr | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154037 | p.Ser692Ile | missense_variant | 0.14 |
katG | 2154461 | p.Ala551Thr | missense_variant | 0.12 |
PPE35 | 2168078 | c.2535C>A | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289156 | p.Arg29Pro | missense_variant | 1.0 |
kasA | 2518185 | p.Ser24Leu | missense_variant | 0.12 |
kasA | 2518790 | p.Ala226Thr | missense_variant | 0.29 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
folC | 2747750 | c.-152G>T | upstream_gene_variant | 0.22 |
pepQ | 2860507 | c.-89C>A | upstream_gene_variant | 0.13 |
ribD | 2987583 | p.Gly249Ser | missense_variant | 0.15 |
Rv2752c | 3066234 | c.-43G>T | upstream_gene_variant | 0.15 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087221 | c.402C>T | synonymous_variant | 0.14 |
Rv3083 | 3448406 | c.-98G>T | upstream_gene_variant | 0.25 |
Rv3083 | 3448864 | p.Val121Met | missense_variant | 0.22 |
Rv3083 | 3448975 | c.472C>A | synonymous_variant | 0.12 |
fprA | 3473958 | c.-49C>A | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474721 | p.Ala239Ser | missense_variant | 0.15 |
fprA | 3474730 | p.Gly242Cys | missense_variant | 0.15 |
Rv3236c | 3612158 | p.Arg320Gln | missense_variant | 0.22 |
ddn | 3986998 | p.Thr52Ile | missense_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040784 | c.-80C>A | upstream_gene_variant | 0.11 |
panD | 4044329 | c.-48C>T | upstream_gene_variant | 0.17 |
embC | 4240123 | c.261C>A | synonymous_variant | 0.13 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embA | 4243181 | c.-52C>T | upstream_gene_variant | 0.2 |
embA | 4243262 | c.30C>T | synonymous_variant | 0.15 |
embA | 4246195 | p.Pro988His | missense_variant | 0.14 |
embB | 4246850 | p.Ala113Ser | missense_variant | 1.0 |
embB | 4247280 | p.Phe256Ser | missense_variant | 0.14 |
embB | 4248813 | p.Leu767Pro | missense_variant | 0.22 |
embB | 4249684 | p.Trp1057* | stop_gained | 0.13 |
aftB | 4268613 | p.Gly75Val | missense_variant | 0.29 |
aftB | 4268852 | c.-16G>A | upstream_gene_variant | 0.22 |
ubiA | 4269710 | p.Gly42Cys | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407973 | p.Val77Gly | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |