Run ID: ERR2245355
Sample name:
Date: 31-03-2023 17:39:17
Number of reads: 1135767
Percentage reads mapped: 99.53
Strain: lineage3.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5599 | c.360G>A | synonymous_variant | 0.15 |
gyrB | 6182 | p.Thr315Ala | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7393 | p.Tyr31Phe | missense_variant | 0.5 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491107 | p.Glu109* | stop_gained | 0.14 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
rpoB | 759724 | c.-83A>T | upstream_gene_variant | 0.5 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761197 | p.Leu464Arg | missense_variant | 0.13 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.91 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764313 | p.Asp315Ala | missense_variant | 0.4 |
rpoC | 765724 | c.2355C>T | synonymous_variant | 0.33 |
rpoC | 766811 | p.Ser1148Ala | missense_variant | 0.29 |
rpoC | 767118 | p.Glu1250Gly | missense_variant | 0.18 |
mmpL5 | 775636 | p.Pro949Thr | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776586 | p.Pro632His | missense_variant | 0.15 |
mmpL5 | 777963 | p.Val173Gly | missense_variant | 0.29 |
mmpS5 | 778602 | c.303delC | frameshift_variant | 0.21 |
mmpL5 | 778741 | c.-261G>T | upstream_gene_variant | 0.18 |
mmpS5 | 779543 | c.-638A>C | upstream_gene_variant | 0.25 |
mmpS5 | 779583 | c.-678T>C | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304938 | p.Glu670* | stop_gained | 0.29 |
fbiC | 1305079 | p.Arg717Trp | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673412 | c.-28G>A | upstream_gene_variant | 0.13 |
inhA | 1673791 | c.-411C>T | upstream_gene_variant | 0.25 |
inhA | 1674212 | p.Leu4Pro | missense_variant | 0.2 |
rpsA | 1833452 | c.-90C>T | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154312 | p.Lys600Asn | missense_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155218 | p.Leu298Phe | missense_variant | 0.25 |
katG | 2155546 | p.Asp189Val | missense_variant | 0.15 |
katG | 2155813 | p.Pro100Gln | missense_variant | 0.18 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169144 | p.Val490Glu | missense_variant | 0.3 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.2 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.22 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289360 | c.-119G>T | upstream_gene_variant | 0.29 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289969 | c.-728G>A | upstream_gene_variant | 0.2 |
pncA | 2290173 | c.-932C>T | upstream_gene_variant | 0.67 |
kasA | 2519055 | p.Ala314Glu | missense_variant | 0.12 |
kasA | 2519102 | p.Gly330Ser | missense_variant | 0.14 |
eis | 2714196 | c.1137T>C | synonymous_variant | 0.25 |
eis | 2715433 | c.-101T>C | upstream_gene_variant | 0.14 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746178 | p.Thr474Asn | missense_variant | 1.0 |
ribD | 2986766 | c.-73G>T | upstream_gene_variant | 0.15 |
ribD | 2987575 | p.Asp246Gly | missense_variant | 0.15 |
Rv2752c | 3066072 | c.120G>T | synonymous_variant | 0.2 |
Rv2752c | 3066360 | c.-169T>G | upstream_gene_variant | 0.22 |
thyX | 3067253 | c.692delA | frameshift_variant | 0.13 |
thyA | 3074462 | p.Tyr4Asn | missense_variant | 0.18 |
thyA | 3074467 | p.Thr2Lys | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474861 | p.Glu285Asp | missense_variant | 0.2 |
whiB7 | 3568828 | c.-149C>A | upstream_gene_variant | 0.15 |
fbiA | 3640814 | p.Glu91Gly | missense_variant | 0.17 |
fbiB | 3642250 | p.Asp239Val | missense_variant | 0.12 |
alr | 3840387 | p.Gln345Leu | missense_variant | 0.4 |
alr | 3840828 | p.Val198Ala | missense_variant | 0.33 |
rpoA | 3878091 | c.417C>T | synonymous_variant | 0.17 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.67 |
ddn | 3986898 | p.Lys19* | stop_gained | 0.29 |
clpC1 | 4038781 | p.Leu642Ile | missense_variant | 0.25 |
clpC1 | 4039694 | c.1011G>A | synonymous_variant | 0.12 |
clpC1 | 4040063 | c.642G>T | synonymous_variant | 0.14 |
clpC1 | 4040194 | p.Leu171Ile | missense_variant | 0.17 |
clpC1 | 4040760 | c.-56C>A | upstream_gene_variant | 0.13 |
embC | 4240059 | p.Thr66Met | missense_variant | 0.12 |
embC | 4240089 | p.Gly76Val | missense_variant | 0.14 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241280 | p.Val473Glu | missense_variant | 0.14 |
embC | 4241292 | p.Leu477Arg | missense_variant | 0.14 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4241961 | p.Leu700Gln | missense_variant | 0.33 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244640 | p.Val470Leu | missense_variant | 0.2 |
embA | 4244716 | p.Trp495Leu | missense_variant | 0.15 |
embA | 4246394 | p.Trp1054Cys | missense_variant | 0.22 |
embB | 4247028 | p.Leu172Gln | missense_variant | 0.33 |
embB | 4247972 | p.Thr487Pro | missense_variant | 0.29 |
embB | 4248007 | c.1494C>A | synonymous_variant | 0.29 |
embB | 4249565 | p.Tyr1018Asp | missense_variant | 0.17 |
aftB | 4268627 | c.210C>T | synonymous_variant | 0.29 |
aftB | 4268826 | p.Val4Gly | missense_variant | 0.17 |
ethA | 4326273 | p.Phe401Val | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |