Run ID: ERR4815267
Sample name:
Date: 01-04-2023 13:46:06
Number of reads: 1033961
Percentage reads mapped: 99.59
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 |
---|---|---|---|---|
gyrB | 5826 | p.Glu196Gly | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7618 | p.Arg106His | missense_variant | 0.12 |
gyrA | 9285 | p.Ala662Thr | missense_variant | 0.15 |
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 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.11 |
rpoB | 760633 | p.Arg276His | missense_variant | 0.11 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766582 | c.3213C>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.1 |
fbiC | 1303160 | p.Gly77Glu | missense_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471683 | n.-163C>T | upstream_gene_variant | 0.12 |
rrl | 1474809 | n.1155delG | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.1 |
rpsA | 1834920 | p.Ala460Glu | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102919 | c.124C>T | synonymous_variant | 0.11 |
katG | 2154105 | p.Glu669Asp | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156044 | p.Val23Ala | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168487 | p.Ile709Asn | missense_variant | 0.17 |
PPE35 | 2169378 | p.Phe412Ser | missense_variant | 0.12 |
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 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726514 | p.Phe108Leu | missense_variant | 0.13 |
Rv2752c | 3065649 | c.543T>C | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474181 | p.Lys59Glu | missense_variant | 1.0 |
fbiA | 3641377 | p.Arg279Trp | missense_variant | 0.1 |
fbiB | 3642075 | p.Asp181Asn | missense_variant | 0.11 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.12 |
clpC1 | 4040152 | p.Gly185Ser | missense_variant | 0.15 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326226 | c.1248C>A | synonymous_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |