Run ID: ERR4819050
Sample name:
Date: 01-04-2023 15:53:49
Number of reads: 480654
Percentage reads mapped: 99.04
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 | 6304 | c.-998C>A | upstream_gene_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7926 | p.Asp209Asn | missense_variant | 0.29 |
gyrA | 8398 | p.Val366Gly | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575570 | p.Ser75Gly | missense_variant | 0.13 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762637 | p.Lys944Arg | missense_variant | 0.13 |
rpoB | 762734 | p.Glu976Asp | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778092 | c.388delT | frameshift_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801150 | c.342G>T | synonymous_variant | 0.18 |
rplC | 801392 | p.Lys195Arg | missense_variant | 0.17 |
fbiC | 1304510 | p.Ala527Val | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673405 | c.-35T>C | upstream_gene_variant | 0.17 |
fabG1 | 1673947 | p.Glu170Lys | missense_variant | 1.0 |
inhA | 1674233 | p.Leu11Gln | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154077 | p.Gln679Lys | missense_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169031 | p.Asp528Asn | missense_variant | 0.12 |
Rv1979c | 2222348 | p.Val273Leu | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288756 | c.486T>C | synonymous_variant | 0.33 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289784 | c.-543C>A | upstream_gene_variant | 0.2 |
kasA | 2518340 | p.Asp76Tyr | missense_variant | 0.29 |
eis | 2715303 | p.Glu10Asp | missense_variant | 0.15 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064846 | p.Val449Ala | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3338986 | c.-132G>C | upstream_gene_variant | 0.12 |
fbiD | 3339076 | c.-42G>A | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612359 | p.Gly253Glu | missense_variant | 0.17 |
fbiB | 3641608 | p.Pro25His | missense_variant | 0.11 |
fbiB | 3642122 | p.Asp196Glu | missense_variant | 0.14 |
clpC1 | 4038706 | p.Asn667Asp | missense_variant | 0.14 |
clpC1 | 4039108 | c.1597C>A | synonymous_variant | 0.33 |
panD | 4044198 | c.84C>T | synonymous_variant | 0.33 |
embC | 4240718 | p.Phe286Leu | missense_variant | 0.5 |
embC | 4240769 | p.Val303Met | missense_variant | 0.17 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244659 | p.Leu476Arg | missense_variant | 0.12 |
embB | 4247971 | c.1458C>T | synonymous_variant | 0.17 |
embB | 4249192 | c.2679C>T | synonymous_variant | 0.22 |
aftB | 4268521 | p.Tyr106His | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |