Run ID: SRR21277521
Sample name:
Date: 04-04-2023 01:19:16
Number of reads: 14222370
Percentage reads mapped: 97.46
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575893 | c.546C>T | synonymous_variant | 0.2 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576223 | c.876G>T | synonymous_variant | 0.12 |
mshA | 576495 | p.Asp383Val | missense_variant | 0.25 |
mshA | 576523 | c.1176G>T | synonymous_variant | 0.22 |
mshA | 576625 | c.1278C>T | synonymous_variant | 0.18 |
ccsA | 619694 | c.-197C>A | upstream_gene_variant | 0.12 |
ccsA | 619838 | c.-53G>T | upstream_gene_variant | 0.1 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766083 | p.Ala905Glu | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.99 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777311 | c.1170C>T | synonymous_variant | 0.17 |
mmpL5 | 777318 | p.Arg388Leu | missense_variant | 0.25 |
mmpL5 | 777371 | c.1110C>A | synonymous_variant | 0.11 |
mmpR5 | 779208 | p.Met73Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303114 | p.Ala62Thr | missense_variant | 0.13 |
fbiC | 1303927 | p.Ala333Thr | missense_variant | 0.12 |
fbiC | 1303941 | c.1011G>A | synonymous_variant | 0.12 |
Rv1258c | 1406308 | p.Arg345Cys | missense_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.95 |
tlyA | 1918104 | c.165G>T | synonymous_variant | 0.11 |
tlyA | 1918578 | c.639G>A | synonymous_variant | 0.18 |
tlyA | 1918591 | c.652C>T | synonymous_variant | 0.1 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155744 | p.Gly123Val | missense_variant | 0.31 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170100 | c.513G>A | synonymous_variant | 0.1 |
PPE35 | 2170363 | p.Glu84* | stop_gained | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746350 | p.Leu417Met | missense_variant | 0.18 |
folC | 2746600 | c.999C>T | synonymous_variant | 0.2 |
pepQ | 2859603 | p.Gly272Phe | missense_variant | 0.14 |
pepQ | 2859606 | c.813G>A | synonymous_variant | 0.11 |
pepQ | 2859611 | p.Leu270Met | missense_variant | 0.12 |
pepQ | 2859925 | p.Pro165Leu | missense_variant | 0.4 |
pepQ | 2859957 | p.Leu154Ile | missense_variant | 0.2 |
pepQ | 2860582 | c.-164A>T | upstream_gene_variant | 0.13 |
thyX | 3067232 | c.714C>T | synonymous_variant | 0.13 |
thyX | 3067414 | p.Ala178Ser | missense_variant | 0.11 |
thyX | 3067427 | c.519G>T | synonymous_variant | 0.21 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087309 | p.Pro164Thr | missense_variant | 0.11 |
ald | 3087313 | p.Gly165Asp | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.99 |
fbiB | 3642244 | p.Ala237Val | missense_variant | 0.15 |
fbiB | 3642359 | c.825C>A | synonymous_variant | 0.1 |
alr | 3841191 | p.Val77Asp | missense_variant | 0.29 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 1.0 |
alr | 3841568 | c.-148G>A | upstream_gene_variant | 1.0 |
alr | 3841570 | c.-151delA | upstream_gene_variant | 1.0 |
alr | 3841574 | c.-154T>G | upstream_gene_variant | 1.0 |
alr | 3841578 | c.-158G>T | upstream_gene_variant | 1.0 |
alr | 3841582 | c.-162A>G | upstream_gene_variant | 1.0 |
alr | 3841584 | c.-164C>A | upstream_gene_variant | 1.0 |
alr | 3841589 | c.-170delG | upstream_gene_variant | 1.0 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 1.0 |
clpC1 | 4038187 | p.Ala840Ser | missense_variant | 0.1 |
embC | 4240641 | p.Arg260Leu | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243503 | p.Ser91Thr | missense_variant | 0.14 |
embA | 4243613 | c.381C>T | synonymous_variant | 0.22 |
embA | 4243886 | p.Met218Ile | missense_variant | 0.12 |
embB | 4246681 | c.168C>A | synonymous_variant | 0.14 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.38 |
embB | 4247855 | p.Gly448Ser | missense_variant | 0.12 |
embB | 4248594 | p.Gly694Asp | missense_variant | 0.16 |
embB | 4248599 | p.Gly696Trp | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267669 | p.Ala390Thr | missense_variant | 0.17 |
aftB | 4267928 | c.909G>C | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |