Run ID: ERR2229180
Sample name:
Date: 31-03-2023 16:46:51
Number of reads: 359706
Percentage reads mapped: 99.61
Strain: lineage4
Drug-resistance: Other
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 |
---|---|---|---|---|---|
pncA | 2289067 | p.Ser59Pro | missense_variant | 0.14 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5984 | p.Arg249Cys | missense_variant | 0.2 |
gyrB | 6329 | p.Glu364Lys | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9077 | c.1776C>A | synonymous_variant | 0.12 |
mshA | 575623 | c.276C>A | synonymous_variant | 0.33 |
ccsA | 619836 | c.-55A>C | upstream_gene_variant | 0.67 |
rpoB | 760417 | p.Ala204Val | missense_variant | 0.14 |
rpoB | 761626 | p.Arg607Leu | missense_variant | 0.2 |
rpoC | 763474 | p.Asn35Lys | missense_variant | 0.2 |
rpoC | 763705 | c.336G>A | synonymous_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775967 | p.Met838Ile | missense_variant | 0.4 |
mmpL5 | 776319 | p.Ser721Thr | missense_variant | 0.25 |
mmpL5 | 777380 | c.1101G>T | synonymous_variant | 0.25 |
mmpL5 | 778432 | p.Arg17Trp | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781567 | p.Thr3Asn | missense_variant | 0.22 |
rplC | 800615 | c.-194G>T | upstream_gene_variant | 0.15 |
fbiC | 1302892 | c.-39C>A | upstream_gene_variant | 0.18 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1303953 | c.1023C>T | synonymous_variant | 0.4 |
fbiC | 1304101 | c.1171C>A | synonymous_variant | 0.12 |
Rv1258c | 1406196 | p.Ala382Glu | missense_variant | 0.17 |
Rv1258c | 1406689 | p.Phe218Val | missense_variant | 0.5 |
Rv1258c | 1407185 | p.Met52Ile | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472890 | n.1045C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473017 | n.1172A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673810 | p.Ser124Leu | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918625 | p.Pro229Gln | missense_variant | 0.29 |
ndh | 2103017 | p.Ala9Glu | missense_variant | 0.22 |
PPE35 | 2167746 | p.Thr956Ser | missense_variant | 0.17 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.19 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
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 | 0.18 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.17 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.15 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.17 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.18 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.25 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.38 |
PPE35 | 2169939 | p.Gly225Ala | missense_variant | 0.2 |
PPE35 | 2169941 | c.672C>T | synonymous_variant | 0.2 |
PPE35 | 2169944 | c.669G>C | synonymous_variant | 0.18 |
PPE35 | 2169947 | c.666T>C | synonymous_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.13 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.18 |
PPE35 | 2170371 | p.Thr81Val | missense_variant | 0.14 |
PPE35 | 2170385 | c.228G>T | synonymous_variant | 0.13 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.14 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.29 |
PPE35 | 2170412 | c.201G>A | synonymous_variant | 0.15 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2986754 | c.-85G>T | upstream_gene_variant | 0.22 |
ald | 3086690 | c.-130G>T | upstream_gene_variant | 0.18 |
fbiD | 3338944 | c.-174G>T | upstream_gene_variant | 0.12 |
fbiD | 3338947 | c.-171G>A | upstream_gene_variant | 0.12 |
fprA | 3475043 | p.Gly346Asp | missense_variant | 0.5 |
Rv3236c | 3612159 | p.Arg320Trp | missense_variant | 1.0 |
fbiA | 3640475 | c.-68C>A | upstream_gene_variant | 0.2 |
fbiB | 3642570 | p.Glu346* | stop_gained | 0.5 |
rpoA | 3877644 | p.Asn288Lys | missense_variant | 0.2 |
clpC1 | 4038357 | p.Asp783Gly | missense_variant | 0.12 |
clpC1 | 4038898 | p.Gly603Ser | missense_variant | 0.25 |
clpC1 | 4039031 | c.1674T>C | synonymous_variant | 0.29 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.15 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.17 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.22 |
embC | 4240162 | c.300C>T | synonymous_variant | 0.67 |
embC | 4241537 | p.Gly559Cys | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.4 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.57 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.57 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.57 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.4 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.4 |
embB | 4249162 | c.2649C>T | synonymous_variant | 0.33 |
embB | 4249168 | c.2655C>T | synonymous_variant | 0.29 |
aftB | 4267346 | p.Asn497Lys | missense_variant | 0.25 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.33 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.33 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |