Run ID: SRR12199421
Sample name:
Date: 03-04-2023 06:38:34
Number of reads: 327834
Percentage reads mapped: 32.54
Strain: lineage1.1.3.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.98 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.3.1 | Indo-Oceanic | NA | RD239 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5122 | c.-118_-117insC | upstream_gene_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7496 | c.195C>T | synonymous_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8828 | p.Asp509Glu | missense_variant | 0.25 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759767 | c.-40G>A | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763131 | p.Pro1109Thr | missense_variant | 0.15 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764541 | p.Val391Asp | missense_variant | 0.2 |
rpoC | 764731 | c.1362G>A | synonymous_variant | 0.12 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777572 | c.909C>T | synonymous_variant | 0.67 |
mmpR5 | 778445 | c.-545G>T | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781479 | c.-81G>C | upstream_gene_variant | 0.14 |
fbiC | 1302914 | c.-17A>T | upstream_gene_variant | 0.33 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.33 |
fbiC | 1303660 | p.Val244Phe | missense_variant | 0.33 |
Rv1258c | 1406721 | p.Gly207Glu | missense_variant | 1.0 |
Rv1258c | 1407436 | c.-96T>A | upstream_gene_variant | 0.25 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471661 | n.-185C>T | upstream_gene_variant | 0.17 |
rrs | 1471670 | n.-176G>A | upstream_gene_variant | 0.18 |
rrl | 1473505 | n.-153G>T | upstream_gene_variant | 0.12 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475745 | n.2088A>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673272 | c.-168C>T | upstream_gene_variant | 0.22 |
rpsA | 1834624 | c.1083G>T | synonymous_variant | 0.5 |
ndh | 2102653 | p.His130Glu | missense_variant | 0.15 |
ndh | 2102955 | p.Ala30Thr | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156355 | c.-244C>T | upstream_gene_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2168150 | c.2463T>C | synonymous_variant | 0.11 |
PPE35 | 2169091 | p.Val508Leu | missense_variant | 0.18 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.12 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.13 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.15 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.12 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.44 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.38 |
PPE35 | 2170363 | p.Glu84Gln | missense_variant | 0.4 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223356 | c.-192C>T | upstream_gene_variant | 0.13 |
pncA | 2288897 | c.345A>G | synonymous_variant | 0.18 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.8 |
eis | 2714846 | p.Val163Ile | missense_variant | 0.2 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3066142 | p.Arg17Gln | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086822 | c.3G>C | start_lost | 0.15 |
ald | 3087627 | p.Asp270Asn | missense_variant | 0.18 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449592 | c.1089C>T | synonymous_variant | 0.18 |
Rv3083 | 3449956 | p.Phe485Leu | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474513 | c.507T>C | synonymous_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568660 | p.Pro7Leu | missense_variant | 0.12 |
Rv3236c | 3613006 | p.Leu37Phe | missense_variant | 0.18 |
Rv3236c | 3613080 | p.Val13Ile | missense_variant | 0.12 |
fbiA | 3640372 | c.-171A>G | upstream_gene_variant | 0.56 |
fbiA | 3641037 | p.Lys165Asn | missense_variant | 0.18 |
alr | 3840221 | c.1200G>A | synonymous_variant | 0.18 |
alr | 3840986 | c.435G>A | synonymous_variant | 0.18 |
alr | 3841253 | c.168C>T | synonymous_variant | 1.0 |
alr | 3841277 | c.144C>T | synonymous_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.4 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.29 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.18 |
clpC1 | 4039909 | p.Glu266* | stop_gained | 0.22 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239978 | p.Leu39Pro | missense_variant | 0.18 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242282 | p.Ser807Ile | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244167 | p.Ala312Val | missense_variant | 0.18 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.17 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.17 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267244 | c.1593T>C | synonymous_variant | 0.2 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338596 | c.-75G>C | 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 | 4407780 | c.423G>A | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
whiB6 | 4338429 | c.-218_92del | frameshift_variant&start_lost | 1.0 |