Run ID: SRR6797439
Sample name:
Date: 04-04-2023 16:09:42
Number of reads: 375561
Percentage reads mapped: 98.76
Strain: lineage1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5041 | c.-199G>T | upstream_gene_variant | 0.25 |
gyrB | 5762 | p.Ala175Thr | missense_variant | 0.25 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.75 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7714 | p.Ala138Val | missense_variant | 0.33 |
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 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575664 | p.Gly106Ala | missense_variant | 1.0 |
mshA | 576000 | p.Asp218Ala | missense_variant | 0.75 |
ccsA | 620425 | p.Val179Ile | missense_variant | 0.5 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764232 | p.Lys288Met | missense_variant | 0.5 |
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 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781427 | c.-133G>A | upstream_gene_variant | 0.67 |
fbiC | 1304106 | c.1176G>A | synonymous_variant | 0.25 |
embR | 1416475 | p.Tyr291* | stop_gained | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474015 | n.358T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476086 | n.2429G>T | non_coding_transcript_exon_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
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 | 2168132 | p.Asp827Glu | missense_variant | 0.25 |
PPE35 | 2168222 | c.2391G>T | synonymous_variant | 0.25 |
PPE35 | 2169092 | c.1521G>T | synonymous_variant | 0.33 |
PPE35 | 2169369 | p.Gly415Ala | missense_variant | 0.67 |
PPE35 | 2169604 | p.Gly337Cys | missense_variant | 0.25 |
PPE35 | 2169671 | c.942C>T | synonymous_variant | 0.12 |
PPE35 | 2170291 | p.Ala108Ser | missense_variant | 0.22 |
Rv1979c | 2221791 | c.1374G>T | synonymous_variant | 0.14 |
Rv1979c | 2222282 | p.Ile295Val | missense_variant | 0.43 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222484 | c.681C>G | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289557 | c.-316C>A | upstream_gene_variant | 0.18 |
pncA | 2289585 | c.-344C>T | upstream_gene_variant | 0.2 |
pncA | 2290199 | c.-958C>G | upstream_gene_variant | 0.67 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
pepQ | 2860418 | p.Val1Met | missense_variant | 0.15 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087113 | c.294C>A | synonymous_variant | 0.17 |
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 |
alr | 3840632 | c.789A>T | synonymous_variant | 0.17 |
alr | 3841253 | c.168C>T | synonymous_variant | 0.43 |
rpoA | 3878306 | p.Gly68Trp | missense_variant | 0.17 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
panD | 4044421 | c.-140G>T | upstream_gene_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240926 | p.Cys355Phe | missense_variant | 0.67 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244840 | c.1608G>A | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246290 | p.Leu1020Ile | missense_variant | 0.18 |
embB | 4246343 | c.-171G>C | upstream_gene_variant | 0.22 |
embA | 4246458 | p.Glu1076* | stop_gained | 0.22 |
embB | 4246771 | c.258C>T | synonymous_variant | 0.4 |
embB | 4247261 | p.Gln250Lys | missense_variant | 0.18 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4268702 | p.Asn45Lys | missense_variant | 0.71 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326007 | c.1467T>C | synonymous_variant | 0.62 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |