Run ID: ERR2229477
Sample name:
Date: 31-03-2023 17:14:40
Number of reads: 728017
Percentage reads mapped: 99.07
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 | 7158 | c.1931_1933delCCG | disruptive_inframe_deletion | 0.14 |
gyrA | 7271 | c.-31A>G | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8777 | p.Asp492Glu | missense_variant | 0.12 |
fgd1 | 491330 | p.Lys183Met | missense_variant | 0.14 |
fgd1 | 491353 | p.Gly191Ser | missense_variant | 0.18 |
ccsA | 619916 | c.28delC | frameshift_variant | 0.33 |
ccsA | 620185 | p.Gly99Ser | missense_variant | 0.15 |
rpoB | 759814 | c.10dupT | frameshift_variant | 0.15 |
rpoB | 761164 | p.Gly453Val | missense_variant | 0.12 |
rpoC | 763369 | c.-1C>T | upstream_gene_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775726 | c.2755C>T | synonymous_variant | 0.15 |
mmpL5 | 775727 | c.2754C>G | synonymous_variant | 0.15 |
mmpL5 | 775736 | c.2745C>G | synonymous_variant | 0.15 |
mmpL5 | 775741 | c.2740C>T | synonymous_variant | 0.17 |
mmpL5 | 775742 | c.2739C>T | synonymous_variant | 0.17 |
mmpL5 | 775747 | p.Met912Leu | missense_variant | 0.17 |
mmpL5 | 775748 | c.2733T>C | synonymous_variant | 0.17 |
mmpL5 | 775851 | p.Ser877Thr | missense_variant | 0.17 |
mmpL5 | 775853 | c.2628C>T | synonymous_variant | 0.17 |
mmpL5 | 775857 | p.Gly875Ala | missense_variant | 0.17 |
mmpL5 | 775862 | c.2619G>C | synonymous_variant | 0.17 |
mmpL5 | 776417 | c.2064G>C | synonymous_variant | 0.18 |
mmpL5 | 776433 | p.Ser683Leu | missense_variant | 0.22 |
mmpL5 | 777566 | c.915C>G | synonymous_variant | 0.25 |
mmpL5 | 777571 | p.Gly304Arg | missense_variant | 0.29 |
mmpL5 | 777573 | p.Phe303Tyr | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407233 | c.108G>A | synonymous_variant | 0.12 |
Rv1258c | 1407235 | c.104_105delTG | frameshift_variant | 0.12 |
Rv1258c | 1407243 | p.Leu33Gln | missense_variant | 0.12 |
atpE | 1461041 | c.-4G>C | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474719 | n.1062G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476172 | n.2515G>C | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.22 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.27 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.27 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.27 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.27 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.47 |
inhA | 1674816 | c.618_619dupGC | frameshift_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918194 | c.255C>A | synonymous_variant | 0.25 |
katG | 2156442 | c.-331G>T | upstream_gene_variant | 0.2 |
katG | 2156466 | c.-355G>T | upstream_gene_variant | 0.13 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.13 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.14 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.14 |
PPE35 | 2168281 | p.Pro778Ser | missense_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.12 |
PPE35 | 2169725 | c.888T>C | synonymous_variant | 0.19 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.5 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.48 |
PPE35 | 2170371 | p.Thr81Val | missense_variant | 0.12 |
PPE35 | 2170385 | c.228G>T | synonymous_variant | 0.12 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.11 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.22 |
PPE35 | 2170412 | c.201G>A | synonymous_variant | 0.18 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.18 |
Rv1979c | 2221963 | p.Ala401Glu | missense_variant | 0.12 |
Rv1979c | 2221987 | p.Leu393Pro | missense_variant | 0.12 |
Rv1979c | 2223136 | p.Ala10Gly | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518240 | c.126C>T | synonymous_variant | 0.14 |
kasA | 2518839 | p.Ala242Gly | missense_variant | 0.12 |
kasA | 2518843 | c.729T>C | synonymous_variant | 0.12 |
kasA | 2519363 | c.1249T>C | stop_lost&splice_region_variant | 0.15 |
folC | 2747575 | c.24G>A | synonymous_variant | 0.29 |
Rv2752c | 3065623 | p.Arg190Gln | missense_variant | 0.12 |
Rv2752c | 3065925 | c.267G>A | synonymous_variant | 0.13 |
thyX | 3067362 | p.Phe195Ser | missense_variant | 0.13 |
whiB7 | 3568469 | p.Phe71Ile | missense_variant | 0.2 |
Rv3236c | 3611962 | p.Asn385Lys | missense_variant | 0.12 |
fbiB | 3640749 | c.-786G>C | upstream_gene_variant | 0.11 |
fbiA | 3640880 | p.Leu113Arg | missense_variant | 0.3 |
fbiA | 3640888 | c.349delC | frameshift_variant | 0.25 |
fbiB | 3641223 | c.-312C>T | upstream_gene_variant | 0.14 |
fbiB | 3642143 | c.611delT | frameshift_variant | 0.25 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.17 |
clpC1 | 4038239 | c.2466T>C | synonymous_variant | 0.11 |
clpC1 | 4039354 | p.Arg451Cys | missense_variant | 0.14 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242655 | c.-578A>G | upstream_gene_variant | 0.22 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.56 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.88 |
embB | 4246555 | c.42G>C | synonymous_variant | 1.0 |
embB | 4246556 | p.Ala15Pro | missense_variant | 1.0 |
embB | 4246563 | p.Leu17Trp | missense_variant | 1.0 |
embB | 4246567 | c.54G>T | synonymous_variant | 1.0 |
embB | 4247678 | c.1166delT | frameshift_variant | 0.12 |
embB | 4247685 | p.Leu391Trp | missense_variant | 0.13 |
embB | 4249646 | c.3136delG | frameshift_variant | 0.13 |
ubiA | 4269365 | p.Tyr157His | missense_variant | 0.12 |
aftB | 4269372 | c.-536G>T | upstream_gene_variant | 0.12 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.11 |
ethR | 4327712 | p.Gly55Asp | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407945 | c.258C>T | synonymous_variant | 0.12 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |