Run ID: SRR21677892
Sample name:
Date: 04-04-2023 02:49:43
Number of reads: 542366
Percentage reads mapped: 98.62
Strain: lineage4.1.1.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6063 | p.Ile275Asn | missense_variant | 0.12 |
gyrA | 7210 | c.-92C>T | upstream_gene_variant | 1.0 |
gyrA | 7279 | c.-23G>T | upstream_gene_variant | 0.12 |
gyrA | 7346 | c.45C>A | synonymous_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7373 | p.Met24Ile | missense_variant | 0.18 |
gyrA | 7569 | p.Ala90Ser | missense_variant | 0.13 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575712 | p.Lys122Arg | missense_variant | 0.14 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776530 | p.Gln651* | stop_gained | 0.14 |
mmpL5 | 776558 | p.Met641Ile | missense_variant | 0.11 |
mmpL5 | 777393 | p.Arg363Gln | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781435 | c.-125G>C | upstream_gene_variant | 1.0 |
rplC | 800815 | c.7C>A | synonymous_variant | 0.13 |
rplC | 800935 | p.Glu43Lys | missense_variant | 0.25 |
fbiC | 1304650 | c.1722delC | frameshift_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473769 | n.112T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474450 | n.793T>C | non_coding_transcript_exon_variant | 0.1 |
inhA | 1673748 | c.-454A>G | upstream_gene_variant | 0.11 |
fabG1 | 1673794 | p.Val119Leu | missense_variant | 0.11 |
inhA | 1674354 | c.153C>A | synonymous_variant | 0.13 |
rpsA | 1834232 | p.Val231Leu | missense_variant | 0.11 |
rpsA | 1834852 | c.1311C>T | synonymous_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918344 | c.405C>T | synonymous_variant | 0.13 |
tlyA | 1918397 | p.Ala153Asp | missense_variant | 0.14 |
ndh | 2102753 | p.Gln97Arg | missense_variant | 0.1 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.23 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.23 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.25 |
Rv1979c | 2222051 | p.Leu372Met | missense_variant | 0.11 |
Rv1979c | 2222067 | c.1098G>T | synonymous_variant | 0.11 |
Rv1979c | 2222070 | c.1095G>A | synonymous_variant | 0.12 |
Rv1979c | 2222100 | c.1065T>C | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288970 | p.Glu91Gly | missense_variant | 0.11 |
pncA | 2289761 | c.-520A>G | upstream_gene_variant | 0.12 |
kasA | 2518618 | c.504G>A | synonymous_variant | 0.17 |
kasA | 2519239 | c.1125A>C | synonymous_variant | 0.14 |
eis | 2714900 | p.Arg145Cys | missense_variant | 0.15 |
eis | 2715476 | c.-144C>A | upstream_gene_variant | 0.12 |
folC | 2746653 | p.Gly316Ser | missense_variant | 0.2 |
folC | 2747482 | c.117G>A | synonymous_variant | 0.13 |
ribD | 2987420 | c.582C>G | synonymous_variant | 0.15 |
thyX | 3067254 | p.Glu231Gly | missense_variant | 0.11 |
thyX | 3067510 | p.Leu146Met | missense_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339460 | p.Gly115Ser | missense_variant | 0.18 |
fbiD | 3339583 | p.Thr156Pro | missense_variant | 0.13 |
Rv3083 | 3449183 | p.Ser227Phe | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641051 | c.511delG | frameshift_variant | 0.12 |
fbiB | 3642519 | p.Asp329Asn | missense_variant | 0.11 |
alr | 3841073 | c.348C>T | synonymous_variant | 0.11 |
ddn | 3987166 | p.Asp108Val | missense_variant | 0.14 |
embC | 4241917 | c.2056dupG | frameshift_variant | 0.12 |
embC | 4242267 | p.Arg802Leu | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244196 | p.Val322Phe | missense_variant | 0.13 |
embA | 4244860 | p.Gly543Glu | missense_variant | 1.0 |
embB | 4245908 | c.-606G>A | upstream_gene_variant | 0.13 |
embA | 4245945 | p.Ile905Phe | missense_variant | 0.12 |
embB | 4246817 | p.Ala102Thr | missense_variant | 0.18 |
embB | 4247606 | c.1093C>T | synonymous_variant | 0.12 |
embB | 4249117 | c.2604G>A | synonymous_variant | 0.13 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
aftB | 4267938 | p.Arg300Leu | missense_variant | 0.22 |
aftB | 4268045 | p.Tyr264* | stop_gained | 0.12 |
ubiA | 4269696 | c.137delA | frameshift_variant | 0.12 |
ethR | 4328090 | p.Arg181Leu | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407798 | c.405G>T | synonymous_variant | 0.96 |