Run ID: SRR4033524
Sample name:
Date: 04-04-2023 06:09:05
Number of reads: 877206
Percentage reads mapped: 99.67
Strain: lineage4.3.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrB | 7220 | p.Ser661Cys | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7605 | p.Pro102Ser | missense_variant | 0.2 |
gyrA | 8948 | c.1647G>A | synonymous_variant | 0.12 |
gyrA | 9099 | p.Leu600Ile | missense_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575507 | p.Thr54Ala | missense_variant | 0.13 |
mshA | 575520 | p.Ala58Val | missense_variant | 0.12 |
mshA | 576201 | p.Arg285His | missense_variant | 0.2 |
rpoB | 762435 | p.Asp877Asn | missense_variant | 0.2 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.4 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765480 | c.2114dupC | frameshift_variant | 0.12 |
rpoC | 767172 | p.Arg1268His | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 779016 | c.-536C>T | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801003 | c.195G>A | synonymous_variant | 0.12 |
fbiC | 1303070 | p.Ala47Val | missense_variant | 0.14 |
fbiC | 1305434 | p.Ala835Val | missense_variant | 0.12 |
Rv1258c | 1406593 | c.747delA | frameshift_variant | 0.13 |
embR | 1417303 | c.45G>A | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673448 | c.-754C>A | upstream_gene_variant | 0.14 |
fabG1 | 1673721 | p.Asp94Glu | missense_variant | 0.22 |
inhA | 1673826 | c.-376C>G | upstream_gene_variant | 0.11 |
rpsA | 1833535 | c.-6delA | upstream_gene_variant | 0.22 |
rpsA | 1834387 | p.Asp282Glu | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155085 | c.1027C>T | synonymous_variant | 0.11 |
katG | 2155719 | c.393G>A | synonymous_variant | 0.18 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518685 | p.Asp191Asn | missense_variant | 0.12 |
kasA | 2519272 | c.1158C>T | synonymous_variant | 0.11 |
ahpC | 2726518 | p.Pro109Gln | missense_variant | 0.25 |
pepQ | 2860299 | c.120C>T | synonymous_variant | 0.13 |
Rv2752c | 3065972 | c.217_219dupGAC | conservative_inframe_insertion | 0.29 |
thyX | 3067695 | p.Gly84Glu | missense_variant | 0.13 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086840 | c.21C>A | synonymous_variant | 0.11 |
ald | 3087903 | p.Pro362Ser | missense_variant | 0.15 |
fbiD | 3339470 | p.Pro118Arg | missense_variant | 0.17 |
Rv3083 | 3448711 | p.Arg70Cys | missense_variant | 0.12 |
Rv3083 | 3448872 | p.Glu123Asp | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474089 | p.Thr28Met | missense_variant | 0.11 |
fprA | 3474640 | c.634T>C | synonymous_variant | 0.12 |
whiB7 | 3568480 | p.Gly67Asp | missense_variant | 0.33 |
fbiA | 3641030 | p.Ser163Ile | missense_variant | 0.15 |
fbiA | 3641124 | p.Ser194Arg | missense_variant | 0.11 |
fbiB | 3642524 | c.990G>T | synonymous_variant | 0.2 |
alr | 3841447 | c.-27A>G | upstream_gene_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038315 | p.Gly797Val | missense_variant | 0.11 |
clpC1 | 4038985 | p.Asp574Tyr | missense_variant | 0.11 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.15 |
panD | 4043865 | c.416delG | frameshift_variant | 0.2 |
embC | 4240759 | c.898delA | frameshift_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245430 | p.Cys733Phe | missense_variant | 0.12 |
embB | 4247649 | p.Ala379Val | missense_variant | 0.14 |
aftB | 4267478 | c.1359G>C | synonymous_variant | 0.17 |
ubiA | 4269469 | p.Pro122Gln | missense_variant | 0.14 |
whiB6 | 4338549 | c.-28G>A | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |