Run ID: SRR3732690
Sample name:
Date: 04-04-2023 05:37:46
Number of reads: 1671335
Percentage reads mapped: 99.62
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
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 | 5754 | c.517_521dupTTCTG | frameshift_variant | 0.17 |
gyrB | 6466 | p.Lys409Asn | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9664 | p.Ala788Glu | missense_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 619856 | c.-35G>T | upstream_gene_variant | 0.14 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620829 | c.939G>T | synonymous_variant | 0.14 |
rpoB | 761066 | c.1260G>T | synonymous_variant | 0.12 |
rpoB | 761145 | p.Arg447Ser | missense_variant | 0.13 |
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 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpR5 | 779023 | p.Ala12Ser | missense_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
mmpS5 | 779630 | c.-725T>C | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304908 | p.Gly660Trp | missense_variant | 0.12 |
fbiC | 1305004 | p.Glu692Lys | missense_variant | 0.2 |
fbiC | 1305051 | c.2121G>T | synonymous_variant | 0.25 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407212 | p.Gln43His | missense_variant | 0.12 |
Rv1258c | 1407453 | c.-113C>A | upstream_gene_variant | 0.11 |
embR | 1417429 | c.-82G>A | upstream_gene_variant | 0.12 |
atpE | 1461115 | p.Ala24Asp | missense_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.77G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473563 | n.-95T>A | upstream_gene_variant | 0.4 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475102 | n.1445C>A | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673870 | p.Ser144Ile | missense_variant | 0.12 |
fabG1 | 1674131 | p.Tyr231Cys | missense_variant | 0.13 |
rpsA | 1833669 | p.Ile43Asn | missense_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834522 | c.981C>T | synonymous_variant | 0.13 |
rpsA | 1834553 | p.Val338Phe | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102114 | p.Ser310Tyr | missense_variant | 0.12 |
ndh | 2102932 | c.111C>T | synonymous_variant | 0.15 |
ndh | 2102967 | c.75delC | frameshift_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168327 | c.2286G>T | synonymous_variant | 0.13 |
Rv1979c | 2222640 | c.525G>T | synonymous_variant | 0.22 |
Rv1979c | 2222683 | p.Trp161Ser | missense_variant | 0.18 |
Rv1979c | 2223268 | c.-104G>T | upstream_gene_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290059 | c.-818T>C | upstream_gene_variant | 0.12 |
ahpC | 2726315 | p.Asp41Glu | missense_variant | 0.12 |
folC | 2746761 | p.Gln280Lys | missense_variant | 0.12 |
pepQ | 2860589 | c.-171G>T | upstream_gene_variant | 0.13 |
Rv2752c | 3067039 | c.-848T>C | upstream_gene_variant | 1.0 |
thyX | 3067612 | p.Lys112* | stop_gained | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086981 | c.162C>T | synonymous_variant | 0.12 |
Rv3083 | 3448603 | p.Leu34Ile | missense_variant | 0.12 |
Rv3083 | 3448730 | p.Ala76Asp | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474573 | c.567C>T | synonymous_variant | 0.14 |
fprA | 3475328 | p.Arg441Leu | missense_variant | 0.12 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3877710 | c.798C>A | synonymous_variant | 0.17 |
rpoA | 3878424 | c.84G>T | synonymous_variant | 0.22 |
clpC1 | 4038768 | p.Arg646Gln | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245800 | p.Trp856Cys | missense_variant | 0.12 |
embB | 4249732 | c.3219C>A | synonymous_variant | 0.14 |
embB | 4249805 | p.Pro1098Thr | missense_variant | 0.17 |
aftB | 4267647 | p.Asp397Gly | missense_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 |