Run ID: SRR6045473
Sample name:
Date: 04-04-2023 11:59:56
Number of reads: 523167
Percentage reads mapped: 98.65
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 | 6536 | p.Thr433Ala | missense_variant | 0.12 |
gyrB | 6930 | p.Ala564Val | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7462 | p.Arg54Leu | missense_variant | 0.15 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7958 | c.657C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575989 | c.642C>T | synonymous_variant | 0.17 |
ccsA | 619814 | c.-77G>T | upstream_gene_variant | 1.0 |
ccsA | 620122 | p.Arg78Trp | missense_variant | 0.18 |
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 | 763649 | p.His94Asn | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777471 | p.Val337Ala | missense_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305411 | c.2481C>T | synonymous_variant | 1.0 |
Rv1258c | 1406316 | p.Gln342Arg | missense_variant | 0.13 |
embR | 1416501 | p.Ala283Thr | missense_variant | 0.11 |
rrs | 1471648 | n.-198A>T | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834435 | c.894G>A | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102818 | c.225G>A | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 1.0 |
PPE35 | 2169047 | p.Ile522Val | missense_variant | 1.0 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169056 | c.1557A>G | synonymous_variant | 1.0 |
PPE35 | 2169741 | p.Asn291Ser | missense_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.4 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289351 | c.-110C>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518174 | c.60A>G | synonymous_variant | 0.18 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.2 |
kasA | 2518199 | p.Ile29Val | missense_variant | 0.18 |
kasA | 2518222 | c.108G>A | synonymous_variant | 0.18 |
kasA | 2518223 | c.109_111delTTGinsCTC | synonymous_variant | 0.18 |
kasA | 2518234 | c.120G>A | synonymous_variant | 0.2 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.15 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.1 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.11 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.14 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.17 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.2 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.25 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.25 |
eis | 2715020 | p.His105Tyr | missense_variant | 0.17 |
eis | 2715063 | c.270G>T | synonymous_variant | 0.22 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2747396 | c.202delC | frameshift_variant | 0.13 |
pepQ | 2859422 | p.Arg333Cys | missense_variant | 0.15 |
pepQ | 2860147 | p.Gly91Asp | missense_variant | 0.12 |
Rv2752c | 3066150 | c.42C>T | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087688 | p.Val290Ala | missense_variant | 0.15 |
fbiD | 3339515 | p.Arg133Leu | missense_variant | 0.18 |
Rv3083 | 3449227 | p.Phe242Leu | missense_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612621 | c.496T>C | synonymous_variant | 0.14 |
fbiB | 3640728 | c.-807G>C | upstream_gene_variant | 0.11 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.13 |
rpoA | 3877896 | c.612G>T | synonymous_variant | 0.17 |
ddn | 3987243 | p.Gln134* | stop_gained | 0.12 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.11 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.11 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.12 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.14 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.14 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.15 |
clpC1 | 4039906 | p.Glu267Lys | missense_variant | 0.12 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.11 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242649 | c.-584G>C | upstream_gene_variant | 0.33 |
embC | 4242702 | p.Ala947Val | missense_variant | 0.13 |
embC | 4242770 | p.Thr970Ser | missense_variant | 0.15 |
embA | 4244417 | c.1185G>A | synonymous_variant | 0.17 |
embA | 4244984 | c.1752G>A | synonymous_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407540 | c.663A>T | synonymous_variant | 0.13 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |