Run ID: ERR2229184
Sample name:
Date: 31-03-2023 16:47:16
Number of reads: 600202
Percentage reads mapped: 99.58
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8229 | p.Val310Phe | missense_variant | 0.12 |
gyrA | 9184 | p.Arg628Leu | missense_variant | 0.13 |
fgd1 | 491239 | p.Asp153Asn | missense_variant | 0.25 |
fgd1 | 491441 | p.Arg220Leu | missense_variant | 0.14 |
ccsA | 620461 | p.Val191Phe | missense_variant | 0.13 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.15 |
rpoB | 762192 | p.Leu796Met | missense_variant | 0.12 |
rpoC | 763940 | p.Ala191Ser | missense_variant | 0.12 |
rpoC | 764970 | p.Ala534Asp | missense_variant | 0.12 |
rpoC | 765447 | p.Gln693Arg | missense_variant | 0.18 |
rpoC | 766905 | p.Ser1179Trp | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775883 | p.Ile866Leu | missense_variant | 0.17 |
mmpL5 | 775927 | c.2554C>T | synonymous_variant | 0.17 |
mmpL5 | 775931 | c.2550C>T | synonymous_variant | 0.17 |
mmpL5 | 776250 | p.Glu744Gly | missense_variant | 0.13 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.17 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.14 |
mmpS5 | 778770 | p.Asp46Asn | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781562 | c.3G>A | start_lost | 0.12 |
rplC | 801374 | p.Asn189Ser | missense_variant | 0.11 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304433 | c.1503G>T | synonymous_variant | 0.18 |
embR | 1416820 | c.528C>A | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473207 | n.1362C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474144 | n.487G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476338 | n.2681C>A | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.31 |
rpsA | 1833448 | c.-94G>A | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.19 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.19 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.13 |
PPE35 | 2170518 | p.Asp32Thr | missense_variant | 0.11 |
PPE35 | 2170540 | c.73C>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518647 | p.Ile178Asn | missense_variant | 0.2 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.43 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.43 |
eis | 2714377 | p.Thr319Met | missense_variant | 0.12 |
pepQ | 2859671 | p.Tyr250Asn | missense_variant | 0.4 |
Rv3236c | 3612743 | p.Thr125Asn | missense_variant | 0.13 |
fbiA | 3640457 | c.-86G>T | upstream_gene_variant | 0.12 |
fbiB | 3641916 | p.Ser128Gly | missense_variant | 0.29 |
clpC1 | 4038986 | p.Asp573Glu | missense_variant | 0.13 |
clpC1 | 4039101 | p.Thr535Asn | missense_variant | 0.12 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.15 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244560 | p.Ile443Asn | missense_variant | 0.22 |
embA | 4246089 | p.Trp953Arg | missense_variant | 0.12 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.22 |
embB | 4247472 | p.Phe320Tyr | missense_variant | 0.22 |
embB | 4248227 | p.Trp572Arg | missense_variant | 0.11 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.14 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.14 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.15 |
ethR | 4326982 | c.-567C>G | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |