Run ID: ERR2229171
Sample name:
Date: 31-03-2023 16:46:52
Number of reads: 466606
Percentage reads mapped: 98.99
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5848 | c.609G>T | synonymous_variant | 0.22 |
gyrA | 7288 | c.-14C>T | upstream_gene_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 490724 | c.-59G>A | upstream_gene_variant | 0.14 |
fgd1 | 490734 | c.-49A>G | upstream_gene_variant | 0.12 |
fgd1 | 490744 | c.-39T>C | upstream_gene_variant | 0.13 |
fgd1 | 491175 | c.393G>C | synonymous_variant | 0.29 |
fgd1 | 491628 | p.Lys282Asn | missense_variant | 0.33 |
rpoB | 759873 | p.Asn23Tyr | missense_variant | 0.2 |
rpoB | 760250 | p.Met148Ile | missense_variant | 0.14 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.29 |
rpoB | 763008 | p.Trp1068Arg | missense_variant | 0.12 |
rpoC | 763436 | c.69delG | frameshift_variant | 0.2 |
rpoC | 766402 | c.3033C>A | synonymous_variant | 0.4 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.22 |
mmpL5 | 776174 | c.2307C>T | synonymous_variant | 0.18 |
mmpL5 | 777150 | p.Asn444Thr | missense_variant | 0.29 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.33 |
mmpL5 | 777173 | c.1308C>T | synonymous_variant | 0.33 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.4 |
mmpL5 | 778398 | p.Ile28Asn | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800627 | c.-182C>A | upstream_gene_variant | 0.17 |
rplC | 801314 | p.Arg169Gln | missense_variant | 0.25 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305121 | p.Asp731Tyr | missense_variant | 0.29 |
fbiC | 1305342 | c.2412C>T | synonymous_variant | 0.33 |
Rv1258c | 1406404 | p.Val313Phe | missense_variant | 0.17 |
Rv1258c | 1406632 | p.Ala237Thr | missense_variant | 0.29 |
Rv1258c | 1407398 | c.-58A>G | upstream_gene_variant | 0.14 |
embR | 1417264 | c.84G>A | synonymous_variant | 0.22 |
embR | 1417370 | c.-23C>A | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473303 | n.1458T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473442 | n.-216G>T | upstream_gene_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.23 |
fabG1 | 1674041 | p.Gly201Val | missense_variant | 0.25 |
rpsA | 1833420 | c.-122C>T | upstream_gene_variant | 0.33 |
rpsA | 1833522 | c.-20G>T | upstream_gene_variant | 0.22 |
rpsA | 1833614 | p.Ala25Thr | missense_variant | 0.15 |
rpsA | 1833670 | c.129C>A | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918492 | p.Phe185Val | missense_variant | 0.17 |
ndh | 2102367 | p.Ala226Pro | missense_variant | 0.67 |
ndh | 2102368 | c.675C>T | synonymous_variant | 0.67 |
ndh | 2102638 | c.405A>G | synonymous_variant | 0.29 |
ndh | 2102846 | p.Gly66Val | missense_variant | 0.14 |
katG | 2154987 | c.1125G>A | synonymous_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168933 | c.1680T>A | synonymous_variant | 0.33 |
PPE35 | 2168974 | c.1638delC | frameshift_variant | 0.17 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.17 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.17 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.15 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.15 |
PPE35 | 2169457 | p.His386Asp | missense_variant | 0.17 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.85 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.85 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.33 |
PPE35 | 2170202 | c.411A>G | synonymous_variant | 0.29 |
PPE35 | 2170207 | p.Ala136Thr | missense_variant | 0.25 |
PPE35 | 2170403 | c.210C>A | synonymous_variant | 0.25 |
PPE35 | 2170406 | c.207A>G | synonymous_variant | 0.33 |
PPE35 | 2170528 | p.Ser29Ala | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289194 | c.48T>A | synonymous_variant | 0.4 |
ahpC | 2726223 | p.Pro11Ser | missense_variant | 0.18 |
ahpC | 2726287 | p.Gly32Asp | missense_variant | 0.22 |
ahpC | 2726712 | p.Cys174Ser | missense_variant | 0.22 |
ald | 3087104 | p.Leu95Phe | missense_variant | 0.2 |
ald | 3087879 | p.Arg354Trp | missense_variant | 1.0 |
Rv3236c | 3612965 | c.151delG | frameshift_variant | 0.22 |
fbiB | 3640632 | c.-903C>A | upstream_gene_variant | 1.0 |
fbiA | 3640880 | p.Leu113Arg | missense_variant | 1.0 |
fbiA | 3640888 | c.349delC | frameshift_variant | 1.0 |
fbiB | 3641382 | c.-153C>T | upstream_gene_variant | 0.25 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.31 |
rpoA | 3878161 | p.Val116Gly | missense_variant | 0.25 |
rpoA | 3878174 | p.Pro112Thr | missense_variant | 0.25 |
rpoA | 3878312 | p.Val66Leu | missense_variant | 0.33 |
clpC1 | 4038649 | p.Gly686Cys | missense_variant | 0.25 |
clpC1 | 4039030 | p.Lys559Glu | missense_variant | 0.33 |
clpC1 | 4039498 | p.Ile403Val | missense_variant | 0.29 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.22 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.5 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242648 | p.Leu929Arg | missense_variant | 0.25 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.25 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.62 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.71 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.71 |
embB | 4247757 | p.Thr415Asn | missense_variant | 1.0 |
embB | 4248419 | p.Leu636Val | missense_variant | 0.5 |
embB | 4248484 | p.Asn657Lys | missense_variant | 0.4 |
aftB | 4266992 | c.1845C>T | synonymous_variant | 1.0 |
aftB | 4267183 | p.Gly552Cys | missense_variant | 0.12 |
ubiA | 4269016 | c.817delG | frameshift_variant | 0.25 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.2 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.2 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.2 |
ethR | 4327207 | c.-342C>T | upstream_gene_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408253 | c.-51A>G | upstream_gene_variant | 0.2 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |