Run ID: ERR2229502
Sample name:
Date: 31-03-2023 17:15:33
Number of reads: 141370
Percentage reads mapped: 98.09
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.86 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7710 | c.409T>C | synonymous_variant | 1.0 |
gyrA | 8597 | c.1296C>T | synonymous_variant | 0.33 |
gyrA | 8963 | c.1662C>T | synonymous_variant | 0.5 |
mmpL5 | 777197 | c.1284C>T | synonymous_variant | 1.0 |
mmpL5 | 777630 | p.Arg284His | missense_variant | 0.67 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471966 | n.121G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472962 | n.1117T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473460 | n.-198G>T | upstream_gene_variant | 0.5 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474307 | n.650G>T | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.38 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.57 |
PPE35 | 2167760 | c.2853G>A | synonymous_variant | 0.57 |
PPE35 | 2167763 | p.Ile950Val | missense_variant | 0.57 |
PPE35 | 2167784 | c.2829C>T | synonymous_variant | 0.33 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169302 | p.Met437Phe | missense_variant | 0.33 |
PPE35 | 2169351 | p.Ala421Tyr | missense_variant | 0.29 |
PPE35 | 2169466 | p.Asn383Asp | missense_variant | 0.17 |
PPE35 | 2169596 | p.Phe339Gly | missense_variant | 0.22 |
PPE35 | 2169748 | p.Ile289Phe | missense_variant | 0.18 |
PPE35 | 2169749 | c.864A>C | synonymous_variant | 0.18 |
PPE35 | 2169937 | c.675dupC | frameshift_variant | 0.29 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 1.0 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 1.0 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.5 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.5 |
PPE35 | 2170177 | c.436C>T | synonymous_variant | 0.5 |
PPE35 | 2170178 | c.435T>A | synonymous_variant | 0.5 |
PPE35 | 2170187 | p.Glu142Gln | missense_variant | 0.25 |
pncA | 2288918 | c.324A>T | synonymous_variant | 1.0 |
ribD | 2986848 | p.Ser4Thr | missense_variant | 0.67 |
Rv2752c | 3065749 | p.His148Leu | missense_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.29 |
alr | 3841589 | c.-170delG | upstream_gene_variant | 0.2 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.22 |
embC | 4240029 | c.168_169insAGC | conservative_inframe_insertion | 0.5 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.67 |
embC | 4241053 | c.1191G>T | synonymous_variant | 0.67 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.6 |
embB | 4247516 | p.Asn335Asp | missense_variant | 1.0 |