Run ID: SRR2101599
Sample name:
Date: 03-04-2023 23:48:39
Number of reads: 617709
Percentage reads mapped: 99.06
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6540 | p.Asp434Gly | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.29 |
mshA | 576373 | c.1026G>A | synonymous_variant | 0.18 |
rpoC | 767156 | p.Gly1263Arg | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776792 | c.1689T>C | synonymous_variant | 0.14 |
mmpL5 | 776889 | p.Ser531Tyr | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475210 | n.1553T>C | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1834520 | p.Ala327Thr | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2168816 | c.1797C>A | synonymous_variant | 0.15 |
PPE35 | 2169415 | p.Gly400Cys | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223346 | c.-182C>T | upstream_gene_variant | 0.11 |
pncA | 2289934 | c.-693C>A | upstream_gene_variant | 0.12 |
ahpC | 2726258 | c.66C>T | synonymous_variant | 0.12 |
folC | 2746588 | c.1011C>T | synonymous_variant | 0.12 |
thyX | 3067285 | p.Ala221Ser | missense_variant | 0.1 |
fprA | 3474269 | p.Val88Asp | missense_variant | 0.11 |
Rv3236c | 3612549 | p.Ala190Ser | missense_variant | 0.17 |
Rv3236c | 3613094 | p.Leu8Ser | missense_variant | 0.17 |
fbiB | 3642231 | c.697C>T | synonymous_variant | 0.11 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
panD | 4044335 | c.-54C>A | upstream_gene_variant | 0.21 |
embC | 4240517 | p.Asp219Asn | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243883 | c.651C>T | synonymous_variant | 0.94 |
embA | 4245780 | p.Ala850Ser | missense_variant | 0.12 |
aftB | 4267473 | p.Gly455Val | missense_variant | 0.15 |
aftB | 4269405 | c.-569G>A | upstream_gene_variant | 0.2 |
ethA | 4326276 | p.Glu400Gln | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |