Run ID: ERR4821980
Sample name:
Date: 01-04-2023 17:34:00
Number of reads: 737317
Percentage reads mapped: 99.53
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 |
---|---|---|---|---|
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 | 491169 | c.387C>T | synonymous_variant | 0.18 |
fgd1 | 491611 | p.Ile277Val | missense_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575946 | p.Thr200Met | missense_variant | 0.23 |
mshA | 576001 | p.Asp218Glu | missense_variant | 0.12 |
mshA | 576008 | p.Ala221Pro | missense_variant | 0.11 |
mshA | 576687 | p.Glu447Gly | missense_variant | 0.17 |
ccsA | 620186 | p.Gly99Asp | missense_variant | 0.25 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776029 | c.2452C>T | synonymous_variant | 0.12 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778278 | p.Ala68Val | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801182 | p.Gly125Asp | missense_variant | 0.12 |
Rv1258c | 1406695 | c.646C>T | synonymous_variant | 0.12 |
Rv1258c | 1406754 | p.Ala196Val | missense_variant | 0.12 |
Rv1258c | 1407102 | p.Ala80Val | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673560 | p.Lys41Leu | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918130 | p.Ser64Leu | missense_variant | 0.14 |
tlyA | 1918532 | p.Val198Ala | missense_variant | 0.14 |
tlyA | 1918537 | p.Asp200Asn | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170533 | p.Ala27Val | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289702 | c.-461T>C | upstream_gene_variant | 0.11 |
pncA | 2289898 | c.-657C>T | upstream_gene_variant | 0.12 |
kasA | 2518754 | p.Arg214Trp | missense_variant | 0.2 |
eis | 2714851 | p.Ser161Asn | missense_variant | 0.13 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746398 | p.Val401Ile | missense_variant | 0.17 |
ribD | 2987100 | p.Val88Met | missense_variant | 0.15 |
Rv2752c | 3066311 | c.-120G>A | upstream_gene_variant | 0.13 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.11 |
thyX | 3067996 | c.-51G>C | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 1.0 |
fbiD | 3339355 | c.238C>T | synonymous_variant | 0.18 |
Rv3083 | 3448839 | c.336G>A | synonymous_variant | 0.14 |
Rv3083 | 3448958 | p.Asp152Val | missense_variant | 0.17 |
Rv3083 | 3448993 | p.Val164Met | missense_variant | 0.15 |
Rv3083 | 3449001 | c.498G>A | synonymous_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474322 | p.Ala106Thr | missense_variant | 0.14 |
fprA | 3474598 | p.Gly198Arg | missense_variant | 0.13 |
fprA | 3474796 | p.His264Tyr | missense_variant | 0.14 |
fprA | 3475110 | c.1104C>T | synonymous_variant | 0.2 |
fprA | 3475160 | p.Asn385Ser | missense_variant | 0.2 |
Rv3236c | 3612140 | p.Ala326Val | missense_variant | 0.12 |
Rv3236c | 3612176 | p.Arg314Gln | missense_variant | 0.13 |
fbiB | 3641508 | c.-27C>T | upstream_gene_variant | 0.14 |
fbiB | 3641730 | p.Asp66Asn | missense_variant | 0.11 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 1.0 |
clpC1 | 4040317 | p.Glu130Lys | missense_variant | 0.12 |
panD | 4044228 | c.54C>G | synonymous_variant | 0.11 |
embC | 4240283 | p.Thr141Ala | missense_variant | 0.11 |
embC | 4240655 | p.Ala265Pro | missense_variant | 0.25 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243699 | p.Pro156Leu | missense_variant | 0.2 |
embA | 4245427 | p.Ser732Asn | missense_variant | 0.11 |
embB | 4246738 | c.225G>T | synonymous_variant | 0.12 |
aftB | 4268848 | c.-12C>T | upstream_gene_variant | 0.14 |
ubiA | 4269268 | p.Ala189Gly | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408319 | c.-117G>A | upstream_gene_variant | 0.12 |
gid | 4408460 | c.-258G>A | upstream_gene_variant | 0.11 |