Run ID: SRR6046284
Sample name:
Date: 04-04-2023 12:14:42
Number of reads: 2779505
Percentage reads mapped: 98.63
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.33 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.35 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.38 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5516 | p.Ile93Val | missense_variant | 0.67 |
gyrB | 6109 | c.870G>A | synonymous_variant | 0.7 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 0.69 |
gyrB | 6717 | p.Ile493Thr | missense_variant | 0.74 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8930 | c.1629C>T | synonymous_variant | 0.62 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.67 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.99 |
fgd1 | 490661 | c.-122_-121insGCGAGC | upstream_gene_variant | 0.56 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491749 | p.Leu323Phe | missense_variant | 0.65 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.41 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.31 |
rpoB | 762352 | c.2557_2562dupGACGAG | conservative_inframe_insertion | 0.39 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.34 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.34 |
mmpL5 | 778086 | c.394dupG | frameshift_variant | 0.64 |
mmpS5 | 778588 | p.Gln106His | missense_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.3 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 0.62 |
Rv1258c | 1406407 | p.Pro312Ser | missense_variant | 0.57 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.35 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475539 | n.1882A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476664 | n.3007T>G | non_coding_transcript_exon_variant | 0.6 |
inhA | 1673680 | c.-522C>G | upstream_gene_variant | 0.63 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.37 |
rpsA | 1834225 | c.684C>T | synonymous_variant | 0.66 |
rpsA | 1834363 | c.822G>A | synonymous_variant | 0.62 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154707 | p.Val469Leu | missense_variant | 0.63 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 0.57 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169279 | c.1312_1333delAACAATGGTGTCTTTTACCGTG | frameshift_variant | 0.57 |
PPE35 | 2170669 | c.-57G>A | upstream_gene_variant | 0.8 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.61 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289978 | c.-737T>G | upstream_gene_variant | 0.6 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.63 |
ahpC | 2726378 | c.186T>A | synonymous_variant | 0.75 |
folC | 2746391 | p.Val403Ala | missense_variant | 0.57 |
Rv2752c | 3067009 | c.-818A>G | upstream_gene_variant | 0.7 |
thyX | 3067812 | p.Gln45Arg | missense_variant | 0.67 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 0.77 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 0.73 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 0.63 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475113 | c.1107G>A | synonymous_variant | 0.68 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.64 |
fprA | 3475323 | c.1317T>C | synonymous_variant | 0.53 |
Rv3236c | 3612694 | c.423T>C | synonymous_variant | 0.66 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.32 |
fbiB | 3641584 | p.Val17Ala | missense_variant | 0.66 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 0.64 |
clpC1 | 4039853 | c.852G>A | synonymous_variant | 0.73 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.6 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.33 |
embA | 4244154 | p.Thr308Ala | missense_variant | 0.49 |
embA | 4244220 | c.988C>T | synonymous_variant | 0.4 |
embB | 4246864 | c.351C>T | synonymous_variant | 0.65 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.49 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.38 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 0.62 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.64 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.67 |
ethA | 4327042 | p.Asp144Asn | missense_variant | 0.79 |
ethA | 4328211 | c.-738A>G | upstream_gene_variant | 0.65 |
whiB6 | 4338269 | p.Gly85Ser | missense_variant | 0.57 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.29 |