Run ID: SRR3732621
Sample name:
Date: 04-04-2023 05:36:45
Number of reads: 1727925
Percentage reads mapped: 99.57
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5349 | p.Thr37Ile | missense_variant | 0.13 |
gyrB | 6195 | p.Gly319Val | missense_variant | 0.14 |
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 | 491192 | p.Gly137Glu | missense_variant | 0.12 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491725 | p.His315Tyr | missense_variant | 0.11 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 575958 | p.Gln204Arg | missense_variant | 0.14 |
ccsA | 620651 | p.Ala254Asp | missense_variant | 0.12 |
ccsA | 620835 | c.945C>T | synonymous_variant | 0.29 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 762503 | c.-867G>T | upstream_gene_variant | 0.12 |
rpoC | 763683 | p.Trp105Leu | missense_variant | 0.13 |
rpoC | 764043 | p.Thr225Asn | missense_variant | 0.12 |
rpoC | 764216 | p.Asn283Asp | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776288 | c.2193C>A | synonymous_variant | 0.12 |
mmpL5 | 776348 | c.2133G>T | synonymous_variant | 0.14 |
mmpL5 | 777019 | p.Asp488His | missense_variant | 0.12 |
mmpL5 | 777106 | p.Ser459Pro | missense_variant | 0.11 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.14 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.11 |
mmpL5 | 779370 | c.-890G>A | upstream_gene_variant | 0.33 |
mmpS5 | 779648 | c.-743C>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800727 | c.-82C>T | upstream_gene_variant | 0.15 |
Rv1258c | 1406556 | p.Trp262Leu | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471974 | n.129T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472104 | n.259G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475450 | n.1793C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476709 | n.3052C>A | non_coding_transcript_exon_variant | 0.25 |
inhA | 1673586 | c.-616C>T | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.12 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.13 |
PPE35 | 2169426 | p.Pro396Gln | missense_variant | 0.12 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289826 | c.-585A>T | upstream_gene_variant | 0.2 |
pncA | 2290224 | c.-983A>G | upstream_gene_variant | 0.15 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714354 | p.Gly327Ser | missense_variant | 0.19 |
thyX | 3067415 | c.530delA | frameshift_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339608 | p.Pro164Leu | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474990 | c.984C>A | synonymous_variant | 0.14 |
fbiB | 3642847 | p.Pro438Leu | missense_variant | 0.15 |
rpoA | 3878695 | c.-189dupT | upstream_gene_variant | 0.18 |
clpC1 | 4038443 | c.2262G>T | synonymous_variant | 0.12 |
clpC1 | 4039998 | p.Gly236Asp | missense_variant | 0.12 |
clpC1 | 4040247 | p.Ala153Asp | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245960 | p.Gln910Lys | missense_variant | 1.0 |
aftB | 4268615 | c.222C>T | synonymous_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407798 | c.405G>T | synonymous_variant | 0.14 |