Run ID: SRR5341217
Sample name:
Date: 04-04-2023 10:07:24
Number of reads: 323448
Percentage reads mapped: 98.9
Strain: lineage4.1.2
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 |
lineage4.1.2 | Euro-American | T;H | None | 0.91 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.33 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490639 | c.-144C>A | upstream_gene_variant | 0.13 |
fgd1 | 490758 | c.-25T>G | upstream_gene_variant | 0.25 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 576077 | c.730C>T | synonymous_variant | 0.33 |
ccsA | 619717 | c.-174G>A | upstream_gene_variant | 0.29 |
ccsA | 620611 | p.Gly241Ser | missense_variant | 0.22 |
ccsA | 620654 | p.Trp255* | stop_gained | 0.2 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.83 |
rpoB | 763134 | p.Gly1110Cys | missense_variant | 0.14 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpR5 | 778469 | c.-521T>C | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304826 | c.1900delT | frameshift_variant | 0.17 |
fbiC | 1305238 | p.His770Asn | missense_variant | 0.25 |
Rv1258c | 1406252 | c.1088delG | frameshift_variant | 0.29 |
Rv1258c | 1406451 | p.Thr297Asn | missense_variant | 0.2 |
rrl | 1473580 | n.-78G>T | upstream_gene_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154143 | p.Phe657Leu | missense_variant | 0.22 |
PPE35 | 2168014 | p.Ala867Thr | missense_variant | 0.22 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.67 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.67 |
Rv1979c | 2221747 | p.Arg473Gln | missense_variant | 0.21 |
Rv1979c | 2223291 | c.-127G>T | upstream_gene_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.83 |
eis | 2715436 | c.-104G>A | upstream_gene_variant | 0.22 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.33 |
folC | 2746745 | p.Val285Gly | missense_variant | 0.5 |
pepQ | 2860023 | c.396C>T | synonymous_variant | 0.5 |
Rv2752c | 3066175 | p.Pro6His | missense_variant | 0.29 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 0.4 |
thyA | 3074316 | p.Phe52Leu | missense_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339143 | c.28_35delATCGGCTT | frameshift_variant | 0.22 |
fbiD | 3339156 | c.40_41insAGCCGATA | frameshift_variant | 0.2 |
Rv3083 | 3448569 | c.66C>T | synonymous_variant | 0.29 |
Rv3083 | 3449566 | p.Gly355Arg | missense_variant | 1.0 |
Rv3083 | 3449759 | p.Thr419Met | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3640773 | c.-762C>T | upstream_gene_variant | 0.15 |
fbiA | 3640880 | c.340dupG | frameshift_variant | 0.2 |
fbiA | 3640888 | c.349delC | frameshift_variant | 0.22 |
alr | 3840764 | c.657G>T | synonymous_variant | 0.29 |
panD | 4043868 | c.414G>T | synonymous_variant | 0.33 |
embC | 4239906 | p.Pro15Leu | missense_variant | 0.2 |
embC | 4239993 | p.Ala44Asp | missense_variant | 0.33 |
embC | 4241473 | c.1611G>T | synonymous_variant | 0.33 |
embC | 4241615 | p.Lys585* | stop_gained | 0.33 |
embC | 4242329 | p.Glu823Lys | missense_variant | 0.83 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243494 | c.262C>T | synonymous_variant | 0.15 |
embA | 4244008 | p.Ala259Glu | missense_variant | 0.33 |
embA | 4244055 | p.Gly275Arg | missense_variant | 0.29 |
embB | 4248226 | c.1713G>T | synonymous_variant | 0.29 |
embB | 4249621 | c.3108G>T | synonymous_variant | 0.25 |
aftB | 4267437 | p.Arg467Gln | missense_variant | 0.22 |
aftB | 4267449 | p.Val463Glu | missense_variant | 0.22 |
ethA | 4327728 | c.-255C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.2 |