Run ID: ERR2514977
Sample name:
Date: 31-03-2023 20:40:41
Number of reads: 850779
Percentage reads mapped: 99.43
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765155 | p.Thr596Ser | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.96 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475895 | n.2238C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103221 | c.-179C>T | upstream_gene_variant | 1.0 |
katG | 2154491 | p.Ala541Thr | missense_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 0.6 |
PPE35 | 2169047 | p.Ile522Val | missense_variant | 0.6 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169056 | c.1557A>G | synonymous_variant | 0.6 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 0.4 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 1.0 |
PPE35 | 2169065 | p.Ala516Ile | missense_variant | 0.4 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 0.5 |
PPE35 | 2169071 | c.1542A>G | synonymous_variant | 0.43 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.18 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064994 | p.Trp400Arg | missense_variant | 0.11 |
Rv2752c | 3065461 | p.Arg244Gln | missense_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475036 | c.1031delT | frameshift_variant | 0.11 |
rpoA | 3878397 | c.111G>A | synonymous_variant | 0.12 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.13 |
panD | 4044203 | p.Thr27Ser | missense_variant | 0.1 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246553 | c.43delG | frameshift_variant | 0.1 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.12 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.13 |
embB | 4249647 | p.Arg1045Pro | missense_variant | 0.12 |
embB | 4249718 | p.Thr1069Ala | missense_variant | 0.13 |
aftB | 4267972 | p.Phe289Leu | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |