Run ID: ERR3077938
Sample name:
Date: 01-04-2023 00:11:48
Number of reads: 816540
Percentage reads mapped: 99.48
Strain: lineage4.2.2.2
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 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
lineage4.2.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761100 | p.Gln432Glu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 0.19 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5556 | p.Gly106Ala | missense_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8688 | p.Ala463Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
ccsA | 620832 | c.942C>A | synonymous_variant | 0.12 |
rpoB | 761031 | p.Gln409Glu | missense_variant | 0.1 |
rpoB | 761248 | p.Glu481Ala | missense_variant | 1.0 |
rpoB | 761489 | c.1683G>A | synonymous_variant | 1.0 |
rpoC | 763711 | c.342G>A | synonymous_variant | 0.14 |
mmpL5 | 775618 | p.Pro955Thr | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777317 | c.1164C>A | synonymous_variant | 0.12 |
mmpL5 | 777435 | p.Ala349Gly | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781822 | p.Lys88Ile | missense_variant | 1.0 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.11 |
rplC | 801338 | p.Val177Ala | missense_variant | 0.1 |
fbiC | 1304474 | p.Leu515Pro | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475259 | n.1602T>G | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918251 | c.312T>C | synonymous_variant | 0.11 |
ndh | 2101865 | p.Trp393Ser | missense_variant | 0.15 |
ndh | 2102520 | p.Val175Phe | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288911 | p.Glu111* | stop_gained | 1.0 |
eis | 2714856 | c.477T>A | synonymous_variant | 0.14 |
ribD | 2987511 | p.Arg225Ser | missense_variant | 0.13 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612214 | c.903C>A | synonymous_variant | 0.12 |
Rv3236c | 3612251 | p.Ser289* | stop_gained | 0.2 |
Rv3236c | 3612617 | p.Pro167Leu | missense_variant | 0.12 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.14 |
ddn | 3986956 | p.Gly38Asp | missense_variant | 0.12 |
panD | 4044414 | c.-133G>T | upstream_gene_variant | 0.13 |
panD | 4044453 | c.-172G>T | upstream_gene_variant | 0.14 |
embC | 4240830 | p.Pro323His | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247387 | p.Val292Leu | missense_variant | 0.1 |
aftB | 4267926 | p.Ala304Glu | missense_variant | 0.12 |
aftB | 4268809 | p.Val10Leu | missense_variant | 0.12 |
whiB6 | 4338403 | p.Arg40Leu | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |