Run ID: SRR6855897
Sample name:
Date: 04-04-2023 17:49:22
Number of reads: 328846
Percentage reads mapped: 99.59
Strain: lineage4.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 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 |
ccsA | 620371 | c.485delC | frameshift_variant | 0.12 |
rpoB | 759693 | c.-114C>A | upstream_gene_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303344 | p.Phe138Leu | missense_variant | 0.15 |
fbiC | 1304880 | c.1950C>G | synonymous_variant | 0.12 |
embR | 1416305 | p.Asn348Ser | missense_variant | 0.11 |
embR | 1416342 | p.Gly336Cys | missense_variant | 0.11 |
embR | 1416809 | p.Ala180Val | missense_variant | 0.1 |
embR | 1417140 | p.Ala70Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673249 | c.-191C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101763 | p.Gly427Asp | missense_variant | 0.11 |
katG | 2154796 | p.Gln439Arg | missense_variant | 0.18 |
katG | 2155705 | p.Pro136Leu | missense_variant | 0.13 |
katG | 2155912 | p.Glu67Val | missense_variant | 0.14 |
PPE35 | 2168139 | p.Ala825Val | missense_variant | 0.14 |
PPE35 | 2169895 | p.Gly240Ser | missense_variant | 0.17 |
PPE35 | 2169910 | p.Asn235Asp | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747022 | p.Val193Ile | missense_variant | 1.0 |
thyX | 3067193 | c.753A>G | stop_lost&splice_region_variant | 0.12 |
thyX | 3067654 | p.His98Tyr | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448894 | p.Tyr131Asp | missense_variant | 1.0 |
Rv3083 | 3449642 | p.Asn380Ser | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568466 | p.Asp72Tyr | missense_variant | 0.18 |
fbiA | 3641026 | p.Glu162Lys | missense_variant | 0.15 |
fbiA | 3641164 | p.Ile208Val | missense_variant | 1.0 |
fbiA | 3641195 | p.Val218Ala | missense_variant | 0.13 |
alr | 3840390 | p.Asp344Gly | missense_variant | 0.1 |
clpC1 | 4039182 | p.Leu508Ser | missense_variant | 0.12 |
panD | 4044149 | p.Thr45Ala | missense_variant | 0.17 |
embC | 4240030 | c.168C>G | synonymous_variant | 0.12 |
embC | 4240182 | p.Ser107Leu | missense_variant | 0.12 |
embC | 4240669 | c.808dupA | frameshift_variant | 0.1 |
embC | 4241995 | c.2134delA | frameshift_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4245932 | c.-582C>A | upstream_gene_variant | 0.25 |
embB | 4247756 | c.1245delC | frameshift_variant | 0.13 |
embB | 4247838 | p.Leu442Pro | missense_variant | 0.11 |
aftB | 4268861 | c.-25T>C | upstream_gene_variant | 0.92 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407934 | p.Leu90Pro | missense_variant | 0.1 |