Run ID: SRR12199451
Sample name:
Date: 03-04-2023 06:41:12
Number of reads: 325947
Percentage reads mapped: 98.62
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6490 | c.-812T>A | upstream_gene_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 762034 | p.Ser743Leu | missense_variant | 0.14 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.22 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.22 |
mmpL5 | 778236 | p.Phe82Ser | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303288 | p.Ser120Gly | missense_variant | 0.2 |
fbiC | 1303803 | c.873C>T | synonymous_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673899 | p.Ala154Ser | missense_variant | 0.33 |
inhA | 1674961 | p.Thr254Ala | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167856 | p.Trp919* | stop_gained | 0.12 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.27 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.3 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.36 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.32 |
PPE35 | 2170294 | p.Pro107Ser | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.22 |
eis | 2714175 | c.1158C>T | synonymous_variant | 0.14 |
eis | 2714603 | p.Val244Leu | missense_variant | 0.25 |
whiB7 | 3568521 | p.Leu53Phe | missense_variant | 0.25 |
whiB7 | 3568712 | c.-33C>T | upstream_gene_variant | 0.15 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
embC | 4240061 | p.Phe67Val | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243534 | p.Gly101Asp | missense_variant | 0.67 |
embA | 4245916 | p.Gln895Leu | missense_variant | 0.4 |
embA | 4246043 | p.Asp937Glu | missense_variant | 0.67 |
embB | 4246770 | p.Asp86Val | missense_variant | 0.33 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.5 |
aftB | 4268412 | p.Gly142Val | missense_variant | 0.18 |
ubiA | 4269059 | p.Ile259Val | missense_variant | 0.33 |
ethA | 4327263 | p.Gly71Arg | missense_variant | 0.22 |
whiB6 | 4338503 | p.Ala7Thr | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407591 | c.612C>T | synonymous_variant | 0.33 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |