Run ID: SRR11972237
Sample name:
Date: 03-04-2023 05:32:56
Number of reads: 226604
Percentage reads mapped: 99.21
Strain: lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
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 | 6566 | p.Ala443Thr | missense_variant | 0.2 |
gyrB | 7020 | p.Gly594Glu | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7945 | p.Thr215Asn | missense_variant | 0.33 |
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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760741 | p.Lys312Arg | missense_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 | 764966 | p.Asn533Asp | missense_variant | 0.18 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765499 | c.2130C>T | synonymous_variant | 0.33 |
rpoC | 767153 | p.Thr1262Ser | missense_variant | 0.25 |
rpoC | 767214 | p.Ala1282Val | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775859 | p.Met874Ile | missense_variant | 0.22 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778843 | c.-363C>T | upstream_gene_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800692 | c.-117C>T | upstream_gene_variant | 0.25 |
rplC | 801073 | p.Ser89Thr | missense_variant | 0.13 |
fbiC | 1304991 | c.2061G>A | synonymous_variant | 0.14 |
fbiC | 1305407 | p.Ser826Leu | missense_variant | 1.0 |
fbiC | 1305501 | c.2571G>A | splice_region_variant&stop_retained_variant | 0.18 |
Rv1258c | 1406112 | p.Asp410Gly | missense_variant | 0.29 |
Rv1258c | 1406354 | p.Gln329His | missense_variant | 0.25 |
Rv1258c | 1406503 | p.Val280Leu | missense_variant | 1.0 |
embR | 1416529 | c.819C>T | synonymous_variant | 0.25 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417355 | c.-8G>T | upstream_gene_variant | 0.22 |
atpE | 1461055 | p.Thr4Ile | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472334 | n.489A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474129 | n.472C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474480 | n.823T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.17 |
inhA | 1673469 | c.-733A>G | upstream_gene_variant | 0.22 |
rpsA | 1834077 | p.Asn179Ile | missense_variant | 0.15 |
rpsA | 1834226 | p.Gly229Cys | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918247 | p.Arg103His | missense_variant | 0.25 |
tlyA | 1918630 | p.Pro231Ser | missense_variant | 0.29 |
ndh | 2102156 | p.Glu296Gly | missense_variant | 0.5 |
ndh | 2103042 | c.1A>T | initiator_codon_variant | 0.13 |
katG | 2156284 | c.-173C>T | upstream_gene_variant | 0.18 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.21 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.43 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.47 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.13 |
PPE35 | 2170049 | c.564G>A | synonymous_variant | 0.14 |
PPE35 | 2170547 | c.66A>C | synonymous_variant | 0.12 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289884 | c.-643G>T | upstream_gene_variant | 0.4 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518633 | c.519G>C | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2747665 | c.-67T>C | upstream_gene_variant | 1.0 |
ribD | 2986708 | c.-131G>A | upstream_gene_variant | 0.22 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3065369 | p.Gln275* | stop_gained | 0.4 |
thyX | 3067829 | c.117C>T | synonymous_variant | 0.29 |
thyA | 3074097 | c.375C>A | synonymous_variant | 0.2 |
thyA | 3074180 | c.291delA | frameshift_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087818 | c.999C>T | synonymous_variant | 0.4 |
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 |
whiB7 | 3568846 | c.-167G>A | upstream_gene_variant | 0.13 |
fbiA | 3641071 | p.Arg177Cys | missense_variant | 0.33 |
fbiB | 3641151 | c.-384G>A | upstream_gene_variant | 0.5 |
alr | 3840723 | p.His233Arg | missense_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.24 |
ddn | 3987282 | p.Val147Leu | missense_variant | 0.22 |
clpC1 | 4038439 | p.Lys756Glu | missense_variant | 0.18 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.4 |
clpC1 | 4039829 | p.Leu292Ile | missense_variant | 0.25 |
clpC1 | 4039931 | c.773delG | frameshift_variant | 0.22 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.14 |
embC | 4240917 | p.Ala352Val | missense_variant | 0.25 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241069 | p.Ala403Thr | missense_variant | 0.33 |
embC | 4241858 | p.Leu666Phe | missense_variant | 0.25 |
embC | 4241934 | p.Ala691Val | missense_variant | 0.22 |
embC | 4242435 | p.Val858Ala | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242973 | p.Glu1037Asp | missense_variant | 0.4 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245707 | p.His825Gln | missense_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247709 | p.Asn399Ser | missense_variant | 0.33 |
embB | 4248537 | p.Leu675Pro | missense_variant | 0.12 |
embB | 4248685 | c.2172C>G | synonymous_variant | 0.13 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269831 | c.3G>T | start_lost | 0.15 |
ubiA | 4269953 | c.-120C>T | upstream_gene_variant | 0.25 |
whiB6 | 4338224 | c.297delC | frameshift_variant | 1.0 |
whiB6 | 4338271 | p.Ser84* | stop_gained | 0.29 |
whiB6 | 4338334 | p.Ala63Glu | missense_variant | 0.29 |
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 | 4407756 | p.Ser149Arg | missense_variant | 0.25 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |