Run ID: SRR19416144
Sample name:
Date: 03-04-2023 21:37:43
Number of reads: 2000978
Percentage reads mapped: 99.23
Strain: lineage1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 5630 | c.391C>T | synonymous_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490649 | c.-134C>A | upstream_gene_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575237 | c.-111C>G | upstream_gene_variant | 0.15 |
mshA | 575320 | c.-28C>A | upstream_gene_variant | 0.22 |
mshA | 575397 | p.Arg17Leu | missense_variant | 0.33 |
mshA | 575509 | c.162C>A | synonymous_variant | 0.14 |
mshA | 576463 | c.1116G>T | synonymous_variant | 1.0 |
ccsA | 619858 | c.-33C>A | upstream_gene_variant | 0.25 |
rpoB | 761504 | c.1698C>A | synonymous_variant | 0.13 |
rpoB | 761690 | c.1884G>A | synonymous_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 766966 | p.Glu1199Asp | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 779316 | c.-836C>A | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102221 | p.Lys274Asp | missense_variant | 0.12 |
ndh | 2102240 | p.Arg268His | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.99 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2170530 | p.Ala28Glu | missense_variant | 0.15 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.99 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746594 | c.1005T>C | synonymous_variant | 0.25 |
ribD | 2987286 | p.Asp150Asn | missense_variant | 0.25 |
ribD | 2987419 | p.Gly194Val | missense_variant | 0.18 |
thyX | 3067952 | c.-7G>T | upstream_gene_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087601 | p.Gly261Val | missense_variant | 1.0 |
fbiD | 3339389 | p.Pro91Gln | missense_variant | 0.14 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448961 | c.462delC | frameshift_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475021 | p.Gly339Arg | missense_variant | 0.2 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiA | 3641459 | p.Val306Glu | missense_variant | 0.12 |
fbiA | 3641524 | p.Gly328* | stop_gained | 0.12 |
fbiB | 3642104 | c.570C>A | synonymous_variant | 0.2 |
fbiB | 3642400 | p.Pro289Gln | missense_variant | 0.13 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_variant | 1.0 |
embC | 4240421 | p.Glu187* | stop_gained | 0.12 |
embC | 4240639 | c.777C>T | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242217 | p.Phe785Leu | missense_variant | 0.22 |
embA | 4242304 | c.-929G>T | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243886 | p.Met218Ile | missense_variant | 0.2 |
embA | 4244172 | p.Leu314Met | missense_variant | 0.11 |
embA | 4244183 | c.951G>T | synonymous_variant | 0.13 |
embA | 4245557 | p.Glu775Asp | missense_variant | 0.14 |
embA | 4245882 | p.Gly884Arg | missense_variant | 0.15 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
aftB | 4267463 | c.1374C>T | synonymous_variant | 1.0 |
aftB | 4267708 | p.Gly377Trp | missense_variant | 0.12 |
aftB | 4268364 | p.Trp158Leu | missense_variant | 0.14 |
aftB | 4268848 | c.-12C>G | upstream_gene_variant | 0.1 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.99 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 0.99 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407848 | p.Ala119Thr | missense_variant | 0.99 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.99 |