Run ID: SRR4033750
Sample name:
Date: 04-04-2023 06:18:16
Number of reads: 1389404
Percentage reads mapped: 99.51
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 | 5936 | p.Ala233Thr | 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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 619984 | p.Leu32Met | missense_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620760 | c.870C>G | synonymous_variant | 1.0 |
rpoB | 760944 | c.1142delA | frameshift_variant | 0.13 |
rpoB | 762523 | c.2720_2722dupTGG | disruptive_inframe_insertion | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763935 | p.Ala189Val | missense_variant | 0.11 |
rpoC | 764491 | c.1122G>A | synonymous_variant | 1.0 |
rpoC | 765173 | p.Ala602Thr | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781619 | p.Lys20Asn | missense_variant | 0.11 |
rplC | 801432 | c.624C>A | synonymous_variant | 0.11 |
fbiC | 1303987 | p.Asp353Tyr | missense_variant | 0.14 |
fbiC | 1304467 | p.Glu513* | stop_gained | 0.13 |
fbiC | 1305055 | c.2126delT | frameshift_variant | 0.13 |
fbiC | 1305216 | c.2286C>T | synonymous_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406998 | p.Ala115Thr | missense_variant | 0.12 |
embR | 1416705 | c.642delC | frameshift_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474978 | n.1321A>T | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102052 | p.Gly331Cys | missense_variant | 0.12 |
ndh | 2102475 | p.Ala190Thr | missense_variant | 0.12 |
katG | 2153933 | p.Ala727Ser | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.3 |
PPE35 | 2170346 | p.Gln89His | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288719 | c.520_522delGAG | conservative_inframe_deletion | 0.15 |
folC | 2747167 | p.Lys144Asn | missense_variant | 1.0 |
folC | 2747353 | c.246C>A | synonymous_variant | 0.14 |
folC | 2747427 | p.Gly58Cys | missense_variant | 0.18 |
folC | 2747579 | p.Gly7Asp | missense_variant | 0.12 |
pepQ | 2859565 | p.Gly285Asp | missense_variant | 0.17 |
ribD | 2987307 | p.Ala157Pro | missense_variant | 0.29 |
ribD | 2987505 | p.Leu223Met | missense_variant | 0.18 |
Rv2752c | 3066237 | c.-46C>A | upstream_gene_variant | 0.12 |
Rv2752c | 3066329 | c.-138C>A | upstream_gene_variant | 0.12 |
thyX | 3067561 | c.384delG | frameshift_variant | 0.22 |
ald | 3086739 | c.-81G>A | upstream_gene_variant | 0.96 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474688 | p.Ala228Thr | missense_variant | 0.18 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641957 | c.423C>A | synonymous_variant | 0.4 |
fbiB | 3642369 | p.Ala279Thr | missense_variant | 0.13 |
clpC1 | 4038396 | c.2308dupG | frameshift_variant | 0.13 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.17 |
embC | 4240435 | c.573C>T | synonymous_variant | 0.15 |
embC | 4241528 | p.Arg556Cys | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246109 | c.-405C>T | upstream_gene_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268499 | p.Arg113His | missense_variant | 0.15 |
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 |