Run ID: SRR5818675
Sample name:
Date: 04-04-2023 11:42:53
Number of reads: 1434232
Percentage reads mapped: 99.24
Strain: lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.99 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrB | 6666 | p.Gln476Leu | missense_variant | 0.12 |
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 | 9047 | c.1746C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9443 | c.2142G>A | synonymous_variant | 1.0 |
gyrA | 9580 | p.Gly760Asp | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
rpoB | 759756 | c.-51C>T | upstream_gene_variant | 0.12 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.14 |
rpoB | 762574 | c.2770delC | frameshift_variant | 0.25 |
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 | 765171 | p.Pro601Leu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
mmpL5 | 777525 | p.Gly319Val | missense_variant | 0.12 |
mmpL5 | 777992 | p.Asn163Lys | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781422 | c.-138A>G | upstream_gene_variant | 0.11 |
Rv1258c | 1407247 | p.Trp32Arg | missense_variant | 0.17 |
Rv1258c | 1407518 | c.-178C>G | upstream_gene_variant | 0.12 |
embR | 1416774 | c.573delC | frameshift_variant | 0.17 |
embR | 1416989 | c.358delA | frameshift_variant | 0.18 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474084 | n.431delA | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475637 | n.1980T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.12 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.12 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102074 | p.Met323Lys | missense_variant | 0.14 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.24 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156149 | c.-38A>T | upstream_gene_variant | 0.11 |
PPE35 | 2167883 | c.2730C>A | synonymous_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2168052 | p.Val854Ala | missense_variant | 0.13 |
PPE35 | 2168863 | c.1750C>T | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.62 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.6 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.12 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.14 |
kasA | 2519344 | c.1230G>T | synonymous_variant | 0.22 |
eis | 2715436 | c.-104G>A | upstream_gene_variant | 0.12 |
eis | 2715440 | c.-108A>C | upstream_gene_variant | 0.15 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3065305 | p.Ala296Val | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087634 | p.Gly272Val | missense_variant | 0.24 |
ald | 3087639 | p.Cys274Ser | missense_variant | 0.22 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3613201 | c.-85C>T | upstream_gene_variant | 0.2 |
alr | 3840713 | c.708C>T | synonymous_variant | 0.96 |
rpoA | 3878497 | p.Ser4* | stop_gained | 0.18 |
ddn | 3987057 | p.Arg72Trp | missense_variant | 0.96 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243790 | c.558G>A | synonymous_variant | 0.4 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embB | 4245902 | c.-612G>A | upstream_gene_variant | 0.14 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.31 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.29 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.29 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4328212 | c.-740delC | upstream_gene_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 | 4407873 | c.330G>T | synonymous_variant | 1.0 |