Run ID: ERR2229476
Sample name:
Date: 31-03-2023 17:14:26
Number of reads: 552087
Percentage reads mapped: 99.41
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 | 6400 | c.-902C>T | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7445 | c.144C>T | synonymous_variant | 0.25 |
gyrA | 7446 | p.Lys49Glu | missense_variant | 0.25 |
gyrA | 9611 | c.2310C>T | synonymous_variant | 0.15 |
fgd1 | 491220 | c.438C>T | synonymous_variant | 0.33 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.18 |
rpoC | 762758 | c.-612G>A | upstream_gene_variant | 0.13 |
rpoC | 765142 | p.Glu591Asp | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775955 | p.Ile842Val | missense_variant | 0.15 |
mmpL5 | 776616 | p.Pro622Leu | missense_variant | 0.15 |
mmpL5 | 776660 | c.1820delT | frameshift_variant | 0.12 |
mmpL5 | 776760 | p.Phe574Tyr | missense_variant | 0.13 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801372 | p.Glu188Asp | missense_variant | 0.12 |
fbiC | 1303295 | p.Tyr122Ser | missense_variant | 0.25 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1417431 | c.-84C>A | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472454 | n.609C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473236 | n.1393dupC | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.22 |
inhA | 1673697 | c.-505G>T | upstream_gene_variant | 0.15 |
rpsA | 1833585 | p.Asp15Gly | missense_variant | 0.12 |
rpsA | 1834778 | p.Glu413Lys | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154370 | p.Val581Ala | missense_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169373 | p.Thr414Ala | missense_variant | 0.12 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.11 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.5 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.6 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.23 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.14 |
PPE35 | 2170164 | p.Ala150Val | missense_variant | 0.14 |
PPE35 | 2170235 | c.378T>C | synonymous_variant | 0.13 |
PPE35 | 2170238 | c.375T>G | synonymous_variant | 0.13 |
PPE35 | 2170244 | c.369G>A | synonymous_variant | 0.13 |
PPE35 | 2170249 | p.Ile122Leu | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288849 | c.390_392delGGT | disruptive_inframe_deletion | 0.14 |
pncA | 2289539 | c.-298C>T | upstream_gene_variant | 0.25 |
pncA | 2289893 | c.-652C>T | upstream_gene_variant | 0.15 |
kasA | 2518026 | c.-89G>T | upstream_gene_variant | 0.13 |
ribD | 2987153 | p.His105Gln | missense_variant | 0.17 |
thyX | 3067426 | p.Val174Met | missense_variant | 0.17 |
thyA | 3074508 | c.-37C>T | upstream_gene_variant | 0.22 |
fprA | 3474151 | p.Val49Met | missense_variant | 0.18 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.19 |
embC | 4240135 | c.273C>A | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243770 | p.Gly180Arg | missense_variant | 0.15 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.43 |
aftB | 4268687 | c.150C>T | synonymous_variant | 0.18 |
aftB | 4268733 | p.Leu35Pro | missense_variant | 0.15 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.12 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.12 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.13 |
ethR | 4327601 | p.Ala18Glu | missense_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 |