Run ID: SRR5535709
Sample name:
Date: 04-04-2023 10:38:47
Number of reads: 1924687
Percentage reads mapped: 99.22
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289192 | p.Gly17Val | missense_variant | 0.33 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5471 | p.Ala78Ser | missense_variant | 0.18 |
gyrB | 5492 | p.Pro85Thr | missense_variant | 0.18 |
gyrA | 7000 | c.-302C>T | upstream_gene_variant | 0.14 |
gyrB | 7195 | p.Met652Ile | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8287 | p.Asn329Thr | missense_variant | 0.25 |
gyrA | 8578 | p.Asp426Gly | missense_variant | 0.17 |
gyrA | 8871 | p.Gly524Arg | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9734 | c.2433A>C | synonymous_variant | 0.17 |
fgd1 | 491353 | p.Gly191Cys | missense_variant | 0.13 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 620404 | p.Leu172Met | missense_variant | 0.17 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760352 | p.Asp182Glu | missense_variant | 0.29 |
rpoB | 760555 | p.Glu250Gly | missense_variant | 1.0 |
rpoB | 762044 | c.2238C>A | synonymous_variant | 0.15 |
rpoC | 762377 | c.-993C>A | upstream_gene_variant | 0.4 |
rpoC | 763142 | c.-228C>A | upstream_gene_variant | 0.18 |
rpoC | 763669 | c.300C>T | synonymous_variant | 0.22 |
rpoC | 763676 | p.His103Asn | missense_variant | 0.2 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765822 | p.Ala818Asp | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775964 | c.2517G>T | synonymous_variant | 0.2 |
mmpL5 | 776236 | p.Thr749Ser | missense_variant | 0.25 |
mmpL5 | 778309 | p.Gln58Lys | missense_variant | 0.17 |
mmpS5 | 778551 | p.Asp119His | missense_variant | 0.14 |
mmpL5 | 778909 | c.-429G>T | upstream_gene_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781691 | p.Lys44Asn | missense_variant | 0.12 |
rplC | 801219 | c.411C>T | synonymous_variant | 0.18 |
fbiC | 1302920 | c.-11G>A | upstream_gene_variant | 0.93 |
fbiC | 1305019 | p.Ala697Thr | missense_variant | 0.17 |
Rv1258c | 1406599 | p.Pro248Thr | missense_variant | 0.2 |
Rv1258c | 1406603 | c.738G>A | synonymous_variant | 0.18 |
Rv1258c | 1406620 | p.Pro241Thr | missense_variant | 0.17 |
Rv1258c | 1407227 | p.Glu38Asp | missense_variant | 0.2 |
embR | 1416352 | c.996C>A | synonymous_variant | 0.22 |
embR | 1417044 | p.Arg102Trp | missense_variant | 0.13 |
embR | 1417150 | c.198G>T | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.4 |
rpsA | 1833868 | p.Tyr109* | stop_gained | 0.13 |
rpsA | 1834764 | p.Glu408Gly | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101922 | p.Ser374* | stop_gained | 0.25 |
ndh | 2102358 | p.Gly229Ser | missense_variant | 0.4 |
ndh | 2102514 | p.Gly177Trp | missense_variant | 0.29 |
ndh | 2102776 | c.267C>T | synonymous_variant | 0.22 |
katG | 2154016 | p.Gly699Val | missense_variant | 0.18 |
katG | 2155243 | p.Ala290Asp | missense_variant | 0.29 |
katG | 2155635 | c.477C>A | synonymous_variant | 0.33 |
PPE35 | 2167874 | c.2739C>A | synonymous_variant | 0.25 |
PPE35 | 2167895 | p.Asn906Lys | missense_variant | 0.25 |
PPE35 | 2168221 | p.Ala798Ser | missense_variant | 0.5 |
PPE35 | 2168236 | p.Ala793Ser | missense_variant | 0.5 |
PPE35 | 2169150 | p.Pro488Gln | missense_variant | 1.0 |
PPE35 | 2170014 | p.Gly200Val | missense_variant | 0.12 |
PPE35 | 2170628 | c.-16C>G | upstream_gene_variant | 0.17 |
Rv1979c | 2223249 | c.-85G>A | upstream_gene_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289522 | c.-281T>G | upstream_gene_variant | 0.29 |
pncA | 2289606 | c.-365G>A | upstream_gene_variant | 0.25 |
pncA | 2289811 | c.-570C>A | upstream_gene_variant | 0.4 |
pncA | 2289848 | c.-607G>T | upstream_gene_variant | 0.2 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518166 | p.Ala18Thr | missense_variant | 0.14 |
kasA | 2518535 | p.Ala141Ser | missense_variant | 0.17 |
eis | 2714243 | p.His364Asn | missense_variant | 0.22 |
folC | 2746277 | p.Asp441Gly | missense_variant | 1.0 |
pepQ | 2860578 | c.-160G>T | upstream_gene_variant | 0.12 |
ribD | 2986649 | c.-190G>T | upstream_gene_variant | 0.15 |
ribD | 2986987 | p.Asp50Ala | missense_variant | 0.13 |
Rv2752c | 3065577 | p.Asn205Lys | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087186 | p.Ala123Thr | missense_variant | 0.22 |
ald | 3087581 | c.762T>C | synonymous_variant | 0.22 |
Rv3083 | 3449054 | p.Gly184Asp | missense_variant | 0.14 |
Rv3083 | 3449069 | p.Ala189Glu | missense_variant | 0.14 |
Rv3083 | 3449613 | p.Lys370Asn | missense_variant | 0.29 |
Rv3083 | 3449660 | p.Trp386Leu | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475141 | p.Val379Ile | missense_variant | 0.22 |
Rv3236c | 3611981 | p.Ala379Asp | missense_variant | 0.15 |
Rv3236c | 3613267 | c.-151G>T | upstream_gene_variant | 0.33 |
fbiA | 3640600 | p.Gln20Lys | missense_variant | 0.18 |
fbiB | 3641010 | c.-525C>A | upstream_gene_variant | 0.27 |
alr | 3840716 | c.705G>T | synonymous_variant | 0.5 |
rpoA | 3878037 | c.471C>A | synonymous_variant | 0.17 |
ddn | 3987214 | p.Pro124Gln | missense_variant | 0.22 |
clpC1 | 4039160 | p.His515Gln | missense_variant | 0.18 |
clpC1 | 4039815 | p.Ala297Asp | missense_variant | 0.15 |
clpC1 | 4040496 | p.Gly70Asp | missense_variant | 0.29 |
embC | 4239886 | c.24C>G | synonymous_variant | 0.14 |
embC | 4240308 | p.Gly149Val | missense_variant | 0.19 |
embC | 4242022 | c.2160G>T | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.97 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244034 | p.Gly268Cys | missense_variant | 0.13 |
embA | 4244833 | p.Val534Ala | missense_variant | 0.17 |
embA | 4245300 | c.2068C>T | synonymous_variant | 0.17 |
embB | 4245527 | c.-987C>T | upstream_gene_variant | 0.2 |
embA | 4245898 | p.Gly889Ala | missense_variant | 0.2 |
embA | 4246038 | p.Ala936Ser | missense_variant | 0.17 |
embB | 4247413 | p.Asp300Glu | missense_variant | 0.33 |
embB | 4248432 | p.Trp640Leu | missense_variant | 0.22 |
embB | 4249383 | p.Pro957Gln | missense_variant | 0.14 |
aftB | 4267383 | p.Ala485Glu | missense_variant | 0.2 |
aftB | 4267925 | c.912G>T | synonymous_variant | 0.22 |
aftB | 4268277 | p.Pro187Leu | missense_variant | 0.17 |
aftB | 4268279 | c.558G>T | synonymous_variant | 0.14 |
aftB | 4268427 | c.409delT | frameshift_variant | 0.12 |
aftB | 4268780 | p.Trp19Cys | missense_variant | 0.18 |
aftB | 4269582 | c.-746C>T | upstream_gene_variant | 0.15 |
aftB | 4269615 | c.-779C>T | upstream_gene_variant | 0.18 |
ubiA | 4269730 | p.Ala35Glu | missense_variant | 0.22 |
ubiA | 4269812 | p.Gln8Lys | missense_variant | 0.23 |
ethA | 4326064 | c.1410C>T | synonymous_variant | 0.29 |
ethA | 4326141 | p.Glu445* | stop_gained | 0.17 |
ethA | 4326497 | p.Arg326Leu | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |