Run ID: SRR12830371
Sample name:
Date: 03-04-2023 06:58:29
Number of reads: 397594
Percentage reads mapped: 99.87
Strain: lineage4.3.4.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.99 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155897 | p.Asp72Gly | missense_variant | 0.1 | isoniazid |
pncA | 2289081 | p.Pro54Leu | missense_variant | 0.14 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8434 | p.Thr378Ser | missense_variant | 1.0 |
gyrA | 8988 | p.Thr563Pro | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576710 | c.1363C>A | synonymous_variant | 0.15 |
rpoC | 763472 | p.Asn35Asp | missense_variant | 0.22 |
rpoC | 763690 | p.Phe107Leu | missense_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.93 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776842 | p.Ala547Ser | missense_variant | 0.13 |
mmpR5 | 778124 | c.-866G>A | upstream_gene_variant | 0.12 |
mmpL5 | 778286 | p.Ser65Arg | missense_variant | 0.14 |
mmpL5 | 778699 | c.-219C>A | upstream_gene_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303720 | p.Gly264Cys | missense_variant | 0.12 |
fbiC | 1303758 | c.828G>T | synonymous_variant | 0.14 |
fbiC | 1304445 | c.1515G>A | synonymous_variant | 0.12 |
Rv1258c | 1406690 | c.651C>G | synonymous_variant | 0.1 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471905 | n.60G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473215 | n.1370A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473778 | n.121G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474143 | n.486T>C | non_coding_transcript_exon_variant | 0.18 |
inhA | 1674643 | p.Asp148Tyr | missense_variant | 0.12 |
rpsA | 1833492 | c.-50G>A | upstream_gene_variant | 0.14 |
rpsA | 1834465 | c.924T>A | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153922 | p.Lys730Asn | missense_variant | 0.13 |
katG | 2156409 | c.-298G>T | upstream_gene_variant | 0.13 |
PPE35 | 2168976 | p.Ala546Val | missense_variant | 0.12 |
PPE35 | 2170125 | p.Val163Ala | missense_variant | 0.11 |
PPE35 | 2170478 | c.135C>T | synonymous_variant | 0.12 |
PPE35 | 2170529 | c.84G>T | synonymous_variant | 0.14 |
Rv1979c | 2222869 | p.Ala99Val | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518013 | c.-102G>T | upstream_gene_variant | 0.11 |
ahpC | 2726470 | c.281delT | frameshift_variant | 0.4 |
ahpC | 2726577 | p.Gly129Ser | missense_variant | 0.18 |
ahpC | 2726657 | c.465A>G | synonymous_variant | 0.12 |
folC | 2746460 | p.Ser380Ile | missense_variant | 0.13 |
Rv2752c | 3065280 | c.912C>A | synonymous_variant | 0.14 |
Rv2752c | 3065293 | p.Val300Ala | missense_variant | 1.0 |
Rv2752c | 3066154 | p.Ser13Tyr | missense_variant | 0.15 |
thyA | 3073820 | p.Leu218Met | missense_variant | 0.18 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074128 | p.Ala115Glu | missense_variant | 0.17 |
ald | 3086706 | c.-114T>C | upstream_gene_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474159 | c.153C>T | synonymous_variant | 0.13 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
fbiA | 3640778 | p.Trp79Leu | missense_variant | 0.15 |
alr | 3841020 | p.Ser134Leu | missense_variant | 0.13 |
rpoA | 3878472 | c.36C>T | synonymous_variant | 0.22 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038834 | p.Phe624Ser | missense_variant | 0.12 |
clpC1 | 4038901 | p.Val602Ile | missense_variant | 0.15 |
clpC1 | 4040499 | p.Gln69Arg | missense_variant | 0.17 |
embC | 4239763 | c.-100C>T | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247884 | c.1371C>A | synonymous_variant | 1.0 |
embB | 4249205 | p.Val898Leu | missense_variant | 0.12 |
ubiA | 4269407 | p.Lys143Glu | missense_variant | 0.12 |
ubiA | 4269424 | p.Ala137Glu | missense_variant | 0.14 |
ethA | 4326441 | p.Asn345Tyr | missense_variant | 0.14 |
ethR | 4327745 | p.Pro66Gln | missense_variant | 0.18 |
ethR | 4327964 | p.Ser139* | stop_gained | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |