Run ID: ERR2229320
Sample name:
Date: 31-03-2023 17:00:30
Number of reads: 952932
Percentage reads mapped: 98.84
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 |
---|---|---|---|---|
gyrB | 6199 | p.Phe320Leu | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.44 |
mshA | 576469 | c.1122G>T | synonymous_variant | 0.15 |
mshA | 576497 | p.Gly384Trp | missense_variant | 0.25 |
ccsA | 620484 | c.594G>A | synonymous_variant | 0.13 |
rpoB | 759749 | c.-57delG | upstream_gene_variant | 0.18 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.15 |
rpoC | 765637 | c.2268C>T | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776008 | p.His825Asp | missense_variant | 0.17 |
mmpL5 | 776730 | p.Tyr584Ser | missense_variant | 0.18 |
mmpL5 | 776739 | p.Ile581Asn | missense_variant | 0.15 |
mmpL5 | 777032 | c.1449C>G | synonymous_variant | 0.13 |
mmpL5 | 777035 | c.1446G>A | synonymous_variant | 0.13 |
mmpL5 | 777042 | p.Arg480Gln | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801303 | c.495G>A | synonymous_variant | 0.2 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304484 | c.1554C>T | synonymous_variant | 0.12 |
fbiC | 1304745 | c.1815C>T | synonymous_variant | 0.12 |
fbiC | 1304935 | p.Ala669Thr | missense_variant | 0.12 |
Rv1258c | 1406599 | p.Pro248Ser | missense_variant | 0.15 |
atpE | 1460851 | c.-194T>C | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.16 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.17 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.2 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.22 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.22 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.36 |
tlyA | 1917785 | c.-155C>T | upstream_gene_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155419 | p.Asn231Lys | missense_variant | 0.13 |
katG | 2155756 | p.Arg119His | missense_variant | 0.2 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.25 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.25 |
PPE35 | 2168143 | p.Phe824Leu | missense_variant | 0.12 |
PPE35 | 2168150 | c.2463T>C | synonymous_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169025 | p.Pro530Ser | missense_variant | 0.12 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.14 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.14 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.2 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.19 |
PPE35 | 2169596 | c.1017T>C | synonymous_variant | 0.14 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.19 |
PPE35 | 2169732 | p.Asn294Ser | missense_variant | 0.21 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.66 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.66 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.17 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.16 |
Rv1979c | 2222683 | p.Trp161Ser | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289813 | c.-573_-572insT | upstream_gene_variant | 0.15 |
pncA | 2289817 | c.-577_-576delTTinsGC | upstream_gene_variant | 0.15 |
pncA | 2290158 | c.-917C>T | upstream_gene_variant | 0.2 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.13 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.14 |
eis | 2714853 | c.480C>T | synonymous_variant | 0.18 |
folC | 2746399 | c.1200C>T | synonymous_variant | 0.15 |
folC | 2746621 | c.978C>G | synonymous_variant | 0.18 |
folC | 2747676 | c.-78C>A | upstream_gene_variant | 0.15 |
ribD | 2986778 | c.-61G>T | upstream_gene_variant | 0.14 |
Rv2752c | 3065598 | c.594G>T | synonymous_variant | 0.17 |
thyA | 3074200 | p.Gly91Val | missense_variant | 0.14 |
fbiB | 3641421 | c.-114C>A | upstream_gene_variant | 0.25 |
fbiB | 3642587 | p.Met351Ile | missense_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.16 |
panD | 4043982 | c.300A>G | synonymous_variant | 0.11 |
embC | 4241152 | c.1290C>A | synonymous_variant | 0.13 |
embC | 4242128 | p.Leu756Met | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.14 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.5 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.57 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.57 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.25 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.25 |
embB | 4249381 | c.2868A>C | synonymous_variant | 0.12 |
aftB | 4268820 | p.Leu6Ser | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |