Run ID: ERR3509865
Sample name:
Date: 01-04-2023 02:32:41
Number of reads: 358283
Percentage reads mapped: 99.8
Strain: lineage4.3.4.2.1
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 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ahpC | 2726141 | c.-52C>T | upstream_gene_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6049 | c.810G>T | synonymous_variant | 0.12 |
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7790 | c.489G>T | synonymous_variant | 0.12 |
gyrA | 8795 | c.1494C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491577 | c.795G>T | synonymous_variant | 0.11 |
rpoB | 760161 | p.Lys119* | stop_gained | 0.18 |
rpoB | 761385 | p.Ala527Pro | missense_variant | 0.33 |
rpoB | 763152 | p.Lys1116Gln | missense_variant | 0.11 |
rpoC | 764731 | c.1362G>T | synonymous_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765080 | p.Gly571Trp | missense_variant | 0.14 |
rpoC | 765499 | c.2130C>A | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775644 | p.Arg946Gln | missense_variant | 0.15 |
mmpL5 | 775856 | c.2625T>C | synonymous_variant | 0.11 |
mmpS5 | 779609 | c.-704C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781761 | p.Pro68Thr | missense_variant | 0.11 |
rplC | 801088 | p.Glu94Lys | missense_variant | 0.29 |
fbiC | 1303631 | p.Pro234His | missense_variant | 0.11 |
fbiC | 1304440 | p.Arg504Ser | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471849 | n.4T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471989 | n.144G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472934 | n.1089C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473283 | n.1440delA | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474329 | n.672G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476667 | n.3010T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476735 | n.3078G>T | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1833877 | c.336C>A | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154958 | p.Arg385Leu | missense_variant | 0.11 |
PPE35 | 2167742 | c.2871C>A | synonymous_variant | 0.14 |
PPE35 | 2169317 | c.1296C>T | synonymous_variant | 0.22 |
PPE35 | 2170568 | c.45C>A | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289173 | c.69T>C | synonymous_variant | 0.11 |
pncA | 2289909 | c.-668G>A | upstream_gene_variant | 1.0 |
eis | 2715465 | c.-133G>T | upstream_gene_variant | 0.13 |
folC | 2746238 | p.Pro454Gln | missense_variant | 0.11 |
Rv2752c | 3065178 | c.1014G>A | synonymous_variant | 0.18 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074294 | p.Leu60Met | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086891 | c.72G>A | synonymous_variant | 0.17 |
Rv3083 | 3448316 | c.-188C>T | upstream_gene_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474842 | p.Lys279Arg | missense_variant | 0.13 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
fbiB | 3641755 | p.Arg74Leu | missense_variant | 0.11 |
fbiB | 3641958 | p.Val142Ile | missense_variant | 0.18 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
rpoA | 3878582 | c.-75C>A | upstream_gene_variant | 0.25 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040857 | c.-153C>A | upstream_gene_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245455 | c.2223C>A | synonymous_variant | 0.11 |
embB | 4246655 | p.Pro48Ser | missense_variant | 0.1 |
ubiA | 4269610 | p.Val75Ala | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |