Run ID: ERR046949
Sample name:
Date: 31-03-2023 08:58:22
Number of reads: 4932191
Percentage reads mapped: 99.47
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 |
---|---|---|---|---|
gyrB | 5472 | p.Ala78Asp | missense_variant | 1.0 |
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 | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.31 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777399 | p.Thr361Arg | missense_variant | 0.18 |
mmpR5 | 779003 | p.Asp5Gly | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461176 | p.Glu44Asp | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473369 | n.1524A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.29 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834315 | c.774C>T | synonymous_variant | 0.99 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168190 | p.Gly808Ala | missense_variant | 1.0 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.41 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.3 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.41 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.28 |
thyX | 3067995 | c.-50A>C | upstream_gene_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339153 | p.Leu12Phe | missense_variant | 0.15 |
fbiD | 3339550 | p.Gly145Trp | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475280 | p.Val425Gly | missense_variant | 0.42 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640957 | p.Gly139Arg | missense_variant | 1.0 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.17 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.18 |
rpoA | 3878238 | p.Asp90Glu | missense_variant | 0.17 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.24 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.3 |
embC | 4239842 | c.-21C>A | upstream_gene_variant | 0.21 |
embC | 4239973 | c.111T>G | synonymous_variant | 0.26 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.21 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.49 |
embC | 4242827 | p.Leu989Val | missense_variant | 0.29 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.99 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.14 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.22 |
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 |