Run ID: ERR4818668
Sample name:
Date: 01-04-2023 15:41:16
Number of reads: 871473
Percentage reads mapped: 99.49
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 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 | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7744 | p.Glu148Val | missense_variant | 0.11 |
gyrA | 8741 | c.1440C>A | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490649 | c.-134C>T | upstream_gene_variant | 0.13 |
fgd1 | 491042 | p.Ala87Asp | missense_variant | 0.12 |
fgd1 | 491259 | c.477T>A | synonymous_variant | 0.12 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575422 | c.75C>T | synonymous_variant | 0.15 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576221 | p.Gly292Arg | missense_variant | 1.0 |
ccsA | 619757 | c.-134G>T | upstream_gene_variant | 0.15 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.23 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766759 | c.3390G>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.21 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673697 | c.-505G>A | upstream_gene_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153947 | p.Gln722Arg | missense_variant | 0.11 |
PPE35 | 2169956 | c.657T>C | synonymous_variant | 0.12 |
PPE35 | 2169964 | p.Leu217Val | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289926 | c.-685A>G | upstream_gene_variant | 0.11 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2715532 | c.-202_-201delCT | upstream_gene_variant | 0.1 |
folC | 2746262 | p.Leu446Arg | missense_variant | 0.12 |
folC | 2747601 | c.-3G>T | upstream_gene_variant | 0.15 |
ribD | 2987099 | c.261C>T | synonymous_variant | 0.14 |
thyX | 3067585 | p.Gly121Cys | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339533 | p.Phe139Ser | missense_variant | 0.13 |
Rv3083 | 3449049 | c.546C>G | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3613081 | c.36C>T | synonymous_variant | 0.11 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.12 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
aftB | 4267922 | c.915G>A | synonymous_variant | 0.15 |
aftB | 4268669 | p.Glu56Asp | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |