Run ID: ERR4819855
Sample name:
Date: 01-04-2023 16:20:31
Number of reads: 433796
Percentage reads mapped: 99.41
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5777 | p.Phe180Leu | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575264 | c.-84C>G | upstream_gene_variant | 0.14 |
mshA | 575356 | c.9T>C | synonymous_variant | 0.33 |
mshA | 575761 | c.414C>T | synonymous_variant | 0.22 |
mshA | 575777 | p.Glu144Gln | missense_variant | 0.33 |
mshA | 576176 | c.829C>T | synonymous_variant | 0.29 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.25 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760568 | c.762G>A | synonymous_variant | 0.18 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764029 | c.660G>A | synonymous_variant | 0.11 |
rpoC | 767226 | p.Pro1286Leu | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777279 | p.Ala401Val | missense_variant | 0.22 |
mmpL5 | 777409 | p.Ile358Phe | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801451 | p.Gly215Ser | missense_variant | 0.15 |
fbiC | 1303263 | c.333G>A | synonymous_variant | 0.12 |
fbiC | 1304655 | c.1725C>T | synonymous_variant | 0.2 |
Rv1258c | 1407439 | c.-99G>A | upstream_gene_variant | 0.2 |
embR | 1417015 | c.333T>C | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918298 | p.Trp120Leu | missense_variant | 0.12 |
katG | 2153936 | p.Ala726Thr | missense_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154861 | c.1251C>T | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167969 | p.Pro882Thr | missense_variant | 0.12 |
PPE35 | 2167998 | p.Pro872Leu | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2290190 | c.-949C>T | upstream_gene_variant | 0.13 |
eis | 2714398 | p.His312Arg | missense_variant | 0.11 |
eis | 2715329 | c.3delG | frameshift_variant | 0.11 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726269 | p.Val26Gly | missense_variant | 0.23 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086803 | c.-17T>C | upstream_gene_variant | 0.13 |
Rv3083 | 3449437 | p.Gly312Ser | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474953 | p.Gln316Leu | missense_variant | 0.11 |
Rv3236c | 3613006 | p.Leu37Phe | missense_variant | 0.15 |
fbiB | 3641629 | p.Ala32Val | missense_variant | 0.13 |
fbiB | 3641722 | c.189delT | frameshift_variant | 0.17 |
alr | 3840256 | p.Glu389* | stop_gained | 0.12 |
ddn | 3987259 | p.Trp139Leu | missense_variant | 0.17 |
panD | 4044011 | p.Ala91Pro | missense_variant | 0.11 |
embC | 4240605 | p.Leu248Pro | missense_variant | 0.14 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242310 | c.-923C>T | upstream_gene_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242921 | p.Ala1020Asp | missense_variant | 0.12 |
embA | 4244383 | p.Leu384Gln | missense_variant | 0.17 |
embA | 4245453 | p.Ala741Thr | missense_variant | 0.11 |
ubiA | 4269028 | p.Gly269Asp | missense_variant | 0.15 |
whiB6 | 4338179 | p.Ser115Thr | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
Rv1258c | 1405770 | c.577_*310del | stop_lost&conservative_inframe_deletion&splice_region_variant | 1.0 |