Run ID: SRR12199470
Sample name:
Date: 03-04-2023 06:42:23
Number of reads: 356291
Percentage reads mapped: 86.23
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 | 5409 | p.Ala57Val | missense_variant | 0.13 |
gyrB | 5676 | p.Trp146Leu | missense_variant | 0.17 |
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 |
mshA | 575799 | p.Val151Ala | missense_variant | 1.0 |
ccsA | 620466 | c.576C>A | synonymous_variant | 0.29 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761966 | p.Trp720Cys | missense_variant | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 767206 | c.3837C>A | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776612 | c.1869C>T | synonymous_variant | 0.17 |
mmpL5 | 776967 | p.Gly505Val | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781449 | c.-111G>T | upstream_gene_variant | 0.18 |
rpsL | 781806 | p.Arg83Cys | missense_variant | 0.14 |
fbiC | 1302995 | p.Asn22Ile | missense_variant | 0.2 |
embR | 1416569 | p.Leu260Pro | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.95 |
rrs | 1472236 | n.391C>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673326 | c.-114C>A | upstream_gene_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155519 | p.Trp198Leu | missense_variant | 0.2 |
katG | 2156344 | c.-233C>A | upstream_gene_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.18 |
PPE35 | 2169695 | c.918A>G | synonymous_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.83 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.83 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.27 |
PPE35 | 2170473 | p.Ser47Leu | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289257 | c.-16A>T | upstream_gene_variant | 0.2 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518516 | c.402C>T | synonymous_variant | 0.25 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.43 |
ahpC | 2726515 | p.Phe108Ser | missense_variant | 0.2 |
Rv2752c | 3066080 | p.Gly38Cys | missense_variant | 0.2 |
Rv2752c | 3066211 | c.-20A>G | upstream_gene_variant | 0.18 |
thyX | 3067673 | p.His91Gln | missense_variant | 0.2 |
thyX | 3068096 | c.-151A>G | upstream_gene_variant | 0.29 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086997 | p.Thr60Gly | missense_variant | 0.4 |
fbiD | 3339668 | p.Gly184Val | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841521 | c.-101G>T | upstream_gene_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.28 |
clpC1 | 4040082 | p.Thr208Ile | missense_variant | 1.0 |
embC | 4239721 | c.-142C>T | upstream_gene_variant | 0.22 |
embC | 4241610 | p.Pro583Gln | missense_variant | 0.4 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245404 | c.2172C>T | synonymous_variant | 0.17 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.33 |
embB | 4249250 | p.Ala913Ser | missense_variant | 0.5 |
embB | 4249588 | c.3075C>T | synonymous_variant | 0.22 |
aftB | 4267342 | p.Gly499Trp | missense_variant | 0.18 |
ubiA | 4269158 | p.Ala226Thr | missense_variant | 0.18 |
ethA | 4327119 | p.His119Tyr | missense_variant | 1.0 |
ethR | 4327243 | c.-306G>A | upstream_gene_variant | 0.4 |
ethA | 4327749 | c.-276G>T | upstream_gene_variant | 0.17 |
ethA | 4328281 | c.-808C>A | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |