Run ID: ERR2228867
Sample name:
Date: 31-03-2023 16:23:46
Number of reads: 107980
Percentage reads mapped: 99.39
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.13 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575637 | p.Asp97Ala | missense_variant | 0.4 |
mshA | 575924 | p.Gly193Arg | missense_variant | 0.29 |
mshA | 576189 | p.Asp281Val | missense_variant | 0.25 |
mshA | 576594 | p.Val416Gly | missense_variant | 0.5 |
rpoB | 760161 | p.Lys119* | stop_gained | 0.33 |
rpoB | 760503 | p.Lys233* | stop_gained | 0.5 |
rpoB | 760565 | c.759A>C | synonymous_variant | 0.5 |
rpoC | 766276 | c.2907C>A | synonymous_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777087 | p.Ile465Ser | missense_variant | 0.67 |
mmpR5 | 778993 | p.Ser2Gly | missense_variant | 0.5 |
mmpR5 | 779432 | p.Asn148Thr | missense_variant | 0.67 |
fbiC | 1304356 | p.Ile476Leu | missense_variant | 0.5 |
fbiC | 1304992 | p.Ser688Ala | missense_variant | 1.0 |
Rv1258c | 1406297 | c.1044A>T | synonymous_variant | 0.67 |
embR | 1416518 | p.Leu277Arg | missense_variant | 1.0 |
rrl | 1476789 | n.3132T>A | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673642 | p.Val68Gly | missense_variant | 0.5 |
rpsA | 1834941 | p.Asp467Ala | missense_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102673 | p.Ser124Pro | missense_variant | 0.4 |
ndh | 2102696 | p.Ile116Thr | missense_variant | 0.4 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168882 | c.1731T>A | synonymous_variant | 0.67 |
PPE35 | 2169022 | p.Gly531Trp | missense_variant | 0.4 |
PPE35 | 2169301 | p.Asn438Tyr | missense_variant | 1.0 |
PPE35 | 2170540 | p.Leu25Val | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289425 | c.-184A>C | upstream_gene_variant | 0.5 |
kasA | 2518144 | c.30T>A | synonymous_variant | 0.5 |
kasA | 2518742 | p.Phe210Val | missense_variant | 0.67 |
ahpC | 2725920 | c.-273A>T | upstream_gene_variant | 0.4 |
thyA | 3073913 | p.Met187Leu | missense_variant | 0.4 |
thyA | 3074528 | c.-57T>G | upstream_gene_variant | 0.67 |
Rv3083 | 3448442 | c.-62A>T | upstream_gene_variant | 0.5 |
fbiB | 3641723 | c.189T>G | synonymous_variant | 0.29 |
fbiB | 3642280 | p.Leu249Arg | missense_variant | 1.0 |
alr | 3840892 | p.Thr177Pro | missense_variant | 0.4 |
alr | 3841288 | p.Ile45Phe | missense_variant | 1.0 |
embC | 4241532 | p.Ile557Asn | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243525 | p.Val98Glu | missense_variant | 0.5 |
embA | 4243824 | p.Thr198Pro | missense_variant | 0.4 |
embA | 4244053 | p.Asp274Ala | missense_variant | 0.4 |
embB | 4247028 | p.Leu172Gln | missense_variant | 1.0 |
embB | 4248111 | p.Val533Gly | missense_variant | 0.33 |
embB | 4249401 | p.Val963Gly | missense_variant | 0.43 |
ethR | 4327285 | c.-264A>T | upstream_gene_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448496 | c.-7_*1408del | transcript_ablation | 1.0 |