Run ID: SRR11972163
Sample name:
Date: 03-04-2023 05:30:33
Number of reads: 452612
Percentage reads mapped: 98.78
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 | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7637 | c.336C>A | synonymous_variant | 0.17 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8647 | p.Gln449Arg | missense_variant | 0.2 |
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 | 9791 | c.2490C>A | synonymous_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575150 | c.-198C>T | upstream_gene_variant | 0.29 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
rpoB | 759832 | p.Thr9Lys | missense_variant | 0.15 |
rpoB | 759939 | p.Pro45Thr | missense_variant | 0.17 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763286 | c.-84G>T | upstream_gene_variant | 0.17 |
rpoC | 763849 | c.480G>A | synonymous_variant | 0.18 |
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 |
rpoC | 766233 | p.Ala955Asp | missense_variant | 0.33 |
rpoC | 766786 | p.Gln1139His | missense_variant | 0.25 |
rpoC | 767206 | c.3837C>T | synonymous_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 0.92 |
mmpL5 | 777560 | c.921C>A | synonymous_variant | 0.4 |
mmpL5 | 777907 | p.Leu192Met | missense_variant | 0.5 |
mmpR5 | 778088 | c.-902C>G | upstream_gene_variant | 1.0 |
mmpR5 | 778094 | c.-896A>G | upstream_gene_variant | 1.0 |
mmpL5 | 778386 | p.Ala32Val | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800922 | c.114C>A | synonymous_variant | 0.13 |
fbiC | 1302898 | c.-33G>T | upstream_gene_variant | 0.22 |
fbiC | 1303434 | p.Asp168Glu | missense_variant | 0.17 |
fbiC | 1305187 | p.Leu753Met | missense_variant | 0.25 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.12 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472193 | n.348A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472415 | n.570T>G | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.3 |
rpsA | 1833855 | p.Lys105Arg | missense_variant | 0.2 |
rpsA | 1834720 | c.1179C>A | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102396 | p.Ala216Val | missense_variant | 0.22 |
ndh | 2102653 | p.His130Glu | missense_variant | 0.15 |
ndh | 2102875 | c.168C>T | synonymous_variant | 0.18 |
katG | 2154240 | p.Met624Ile | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2168946 | p.Pro556Leu | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.14 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.13 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.13 |
PPE35 | 2170357 | p.Ala86Thr | missense_variant | 0.18 |
PPE35 | 2170518 | p.Asp32Ala | missense_variant | 0.18 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288821 | p.Gln141Lys | missense_variant | 0.2 |
pncA | 2289272 | c.-31C>T | upstream_gene_variant | 0.67 |
pncA | 2290179 | c.-938G>T | upstream_gene_variant | 0.4 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519159 | p.Ala349Ser | missense_variant | 0.2 |
eis | 2714742 | p.Trp197Cys | missense_variant | 0.15 |
eis | 2714827 | p.Thr169Asn | missense_variant | 0.25 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.24 |
ahpC | 2726631 | p.Val147Phe | missense_variant | 0.14 |
folC | 2747427 | p.Gly58Ser | missense_variant | 0.4 |
folC | 2747551 | c.48C>A | synonymous_variant | 0.2 |
pepQ | 2860485 | c.-67C>A | upstream_gene_variant | 0.12 |
ribD | 2986760 | c.-79C>A | upstream_gene_variant | 0.25 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3065032 | p.Gly387Val | missense_variant | 0.22 |
Rv2752c | 3065089 | p.Ala368Glu | missense_variant | 0.2 |
Rv2752c | 3065305 | p.Ala296Val | missense_variant | 1.0 |
Rv2752c | 3065847 | p.Lys115Asn | missense_variant | 0.22 |
Rv2752c | 3066080 | p.Gly38Cys | missense_variant | 0.13 |
thyA | 3074653 | c.-182G>T | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449301 | c.798G>T | synonymous_variant | 0.22 |
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 | 3613197 | c.-81G>A | upstream_gene_variant | 0.2 |
fbiA | 3640832 | p.Val97Ala | missense_variant | 0.2 |
rpoA | 3878578 | c.-71C>A | upstream_gene_variant | 0.29 |
ddn | 3987057 | p.Arg72Trp | missense_variant | 1.0 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.18 |
clpC1 | 4040335 | p.Leu124Val | missense_variant | 0.25 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240288 | c.426C>A | synonymous_variant | 0.17 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242099 | p.Gly746Asp | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244305 | p.Arg358Leu | missense_variant | 0.25 |
embB | 4245671 | c.-843C>A | upstream_gene_variant | 0.22 |
embA | 4245882 | p.Gly884Cys | missense_variant | 0.29 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246236 | p.Leu1002Ile | missense_variant | 0.33 |
embB | 4246723 | c.210G>T | synonymous_variant | 1.0 |
embB | 4247546 | p.Asp345Tyr | missense_variant | 0.4 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249329 | p.Met939Arg | missense_variant | 0.2 |
embB | 4249395 | p.Ile961Thr | missense_variant | 0.12 |
aftB | 4267250 | p.Asp529Glu | missense_variant | 0.15 |
aftB | 4267430 | c.1407G>T | synonymous_variant | 0.2 |
aftB | 4267953 | p.Ala295Val | missense_variant | 0.33 |
aftB | 4268424 | p.Gly138Val | missense_variant | 0.17 |
ubiA | 4269325 | p.Ile170Thr | missense_variant | 0.12 |
ubiA | 4269346 | p.Ala163Val | missense_variant | 0.17 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269467 | p.Asn123His | missense_variant | 0.25 |
aftB | 4269471 | c.-635C>G | upstream_gene_variant | 0.25 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.83 |
aftB | 4269636 | c.-800C>A | upstream_gene_variant | 0.4 |
ethA | 4326482 | p.Arg331Leu | missense_variant | 0.33 |
ethR | 4327051 | c.-498G>A | upstream_gene_variant | 0.29 |
whiB6 | 4338384 | p.Asp46Glu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338617 | c.-96C>A | upstream_gene_variant | 0.18 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |