Run ID: SRR4037686
Sample name:
Date: 04-04-2023 07:35:46
Number of reads: 560562
Percentage reads mapped: 99.52
Strain: lineage2.2.1
Drug-resistance: Other
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 |
---|---|---|---|---|---|
ethA | 4327294 | p.Tyr60* | stop_gained | 0.13 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6248 | p.Leu337Ile | missense_variant | 0.12 |
gyrB | 6886 | p.Phe549Leu | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7499 | c.198G>T | synonymous_variant | 0.25 |
gyrA | 7529 | c.228G>T | synonymous_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7594 | p.Arg98His | missense_variant | 0.22 |
gyrA | 8826 | p.Asp509Tyr | missense_variant | 0.4 |
gyrA | 8843 | p.Glu514Asp | missense_variant | 0.5 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9798 | p.Ala833Ser | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575378 | p.Gly11Trp | missense_variant | 0.2 |
mshA | 575643 | p.Pro99Gln | missense_variant | 0.2 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620211 | p.Trp107Cys | missense_variant | 0.22 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761164 | p.Gly453Val | missense_variant | 0.14 |
rpoB | 762080 | c.2274G>T | synonymous_variant | 0.18 |
rpoC | 762488 | c.-882G>T | upstream_gene_variant | 0.18 |
rpoB | 762903 | p.Asp1033Tyr | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763088 | c.-282C>A | upstream_gene_variant | 0.17 |
rpoC | 764209 | c.840C>A | synonymous_variant | 0.13 |
rpoC | 764906 | p.Glu513* | stop_gained | 0.18 |
rpoC | 764993 | p.Ala542Ser | missense_variant | 0.2 |
rpoC | 765000 | p.His544Leu | missense_variant | 0.2 |
rpoC | 765679 | c.2310C>A | synonymous_variant | 0.15 |
rpoC | 766659 | p.Arg1097Leu | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775841 | c.2640G>T | synonymous_variant | 0.22 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776900 | p.Asn527Lys | missense_variant | 0.15 |
mmpL5 | 777461 | c.1020G>A | synonymous_variant | 0.33 |
mmpL5 | 777499 | c.982C>A | synonymous_variant | 0.25 |
mmpL5 | 777915 | p.Ser189* | stop_gained | 0.17 |
mmpS5 | 779535 | c.-630C>A | upstream_gene_variant | 0.13 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781597 | p.Arg13Leu | missense_variant | 0.5 |
rpsL | 781638 | p.Ser27Gly | missense_variant | 0.4 |
rpsL | 781679 | c.120C>A | synonymous_variant | 0.33 |
rplC | 800813 | p.Ala2Val | missense_variant | 0.17 |
rplC | 801303 | c.495G>T | synonymous_variant | 0.25 |
fbiC | 1302967 | p.Pro13Ser | missense_variant | 0.15 |
fbiC | 1305397 | p.Glu823* | stop_gained | 0.25 |
Rv1258c | 1406461 | p.Ala294Ser | missense_variant | 0.22 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416962 | p.Gly129Asp | missense_variant | 0.17 |
embR | 1417326 | p.Glu8* | stop_gained | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473609 | n.-49G>T | upstream_gene_variant | 0.12 |
rrl | 1474238 | n.581G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474503 | n.846G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474911 | n.1254G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475595 | n.1938G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476009 | n.2352G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673944 | p.Arg169Ser | missense_variant | 0.17 |
rpsA | 1834110 | p.Trp190* | stop_gained | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834444 | c.903C>A | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918337 | p.Arg133Leu | missense_variant | 0.15 |
tlyA | 1918611 | c.672C>A | synonymous_variant | 0.29 |
ndh | 2102118 | p.Leu309Met | missense_variant | 0.22 |
ndh | 2102216 | p.Trp276Leu | missense_variant | 0.13 |
ndh | 2102833 | c.210G>A | synonymous_variant | 0.25 |
katG | 2154317 | p.Gly599Arg | missense_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156335 | c.-224C>A | upstream_gene_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168476 | p.Pro713Thr | missense_variant | 0.2 |
PPE35 | 2168947 | p.Pro556Thr | missense_variant | 0.15 |
PPE35 | 2170101 | p.Pro171Gln | missense_variant | 0.25 |
PPE35 | 2170103 | c.510C>A | synonymous_variant | 0.22 |
Rv1979c | 2222055 | p.Asp370Glu | missense_variant | 0.13 |
Rv1979c | 2222074 | p.Pro364Gln | missense_variant | 0.14 |
Rv1979c | 2222136 | p.Lys343Asn | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289801 | c.-560C>T | upstream_gene_variant | 0.4 |
kasA | 2519207 | p.Gly365Cys | missense_variant | 0.18 |
eis | 2714421 | c.912A>G | synonymous_variant | 0.22 |
eis | 2714621 | p.Val238Phe | missense_variant | 0.25 |
eis | 2714673 | c.660C>A | synonymous_variant | 0.4 |
eis | 2714969 | p.Glu122* | stop_gained | 0.33 |
ahpC | 2726606 | c.414C>T | synonymous_variant | 0.4 |
folC | 2746260 | p.Val447Phe | missense_variant | 0.29 |
ribD | 2986989 | p.Gly51Cys | missense_variant | 0.18 |
ribD | 2987183 | c.345G>T | synonymous_variant | 0.17 |
ribD | 2987254 | p.Ala139Glu | missense_variant | 0.22 |
Rv2752c | 3064565 | p.Glu543* | stop_gained | 0.22 |
Rv2752c | 3064808 | p.Leu462Met | missense_variant | 0.12 |
Rv2752c | 3065441 | p.Ala251Ser | missense_variant | 0.22 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.4 |
thyA | 3073985 | p.Leu163Ile | missense_variant | 0.25 |
thyA | 3074625 | c.-154G>T | upstream_gene_variant | 0.17 |
ald | 3086653 | c.-167C>A | upstream_gene_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087300 | p.Gly161Cys | missense_variant | 0.22 |
fbiD | 3339278 | p.Gly54Val | missense_variant | 1.0 |
fbiD | 3339384 | c.267C>A | synonymous_variant | 0.18 |
Rv3083 | 3448500 | c.-4A>G | upstream_gene_variant | 0.22 |
Rv3083 | 3448586 | p.Pro28His | missense_variant | 0.14 |
Rv3083 | 3448748 | p.Arg82Leu | missense_variant | 0.17 |
Rv3083 | 3449883 | p.Trp460Cys | missense_variant | 0.17 |
Rv3083 | 3449884 | p.Arg461Gly | missense_variant | 0.17 |
fprA | 3473923 | c.-84G>T | upstream_gene_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568499 | p.Glu61* | stop_gained | 0.5 |
whiB7 | 3568532 | c.148C>A | synonymous_variant | 0.4 |
whiB7 | 3568626 | c.53delT | frameshift_variant | 1.0 |
Rv3236c | 3612131 | p.Ala329Glu | missense_variant | 0.15 |
Rv3236c | 3612153 | p.Gly322Trp | missense_variant | 0.15 |
Rv3236c | 3612630 | p.Ala163Ser | missense_variant | 0.18 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612973 | c.144C>A | synonymous_variant | 0.25 |
fbiB | 3641709 | c.175C>A | synonymous_variant | 0.25 |
fbiB | 3642698 | c.1164G>T | synonymous_variant | 0.29 |
fbiB | 3642708 | p.Gly392Trp | missense_variant | 0.29 |
alr | 3840636 | p.Pro262Gln | missense_variant | 0.2 |
alr | 3841243 | p.Gln60Lys | missense_variant | 0.29 |
alr | 3841586 | c.-166G>T | upstream_gene_variant | 0.15 |
rpoA | 3877572 | c.936G>A | synonymous_variant | 0.33 |
clpC1 | 4038175 | p.Glu844* | stop_gained | 0.25 |
embC | 4240720 | p.Phe286Leu | missense_variant | 0.17 |
embC | 4241228 | p.Leu456Ile | missense_variant | 0.17 |
embC | 4241236 | c.1374C>A | synonymous_variant | 0.17 |
embC | 4241709 | p.Arg616Leu | missense_variant | 0.18 |
embC | 4241952 | p.Arg697Met | missense_variant | 0.13 |
embC | 4242058 | c.2196G>T | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242739 | c.-494C>A | upstream_gene_variant | 0.18 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.4 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243728 | p.Lys166Glu | missense_variant | 0.22 |
embB | 4248066 | p.Trp518Leu | missense_variant | 0.22 |
embB | 4248268 | c.1755G>C | synonymous_variant | 0.29 |
aftB | 4267046 | p.Phe597Leu | missense_variant | 0.2 |
aftB | 4267073 | c.1764C>A | synonymous_variant | 0.17 |
aftB | 4267088 | c.1749C>A | synonymous_variant | 0.15 |
aftB | 4267096 | p.Pro581Thr | missense_variant | 0.22 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268177 | c.660G>A | synonymous_variant | 0.15 |
ubiA | 4269117 | p.Glu239Asp | missense_variant | 0.4 |
ethA | 4326305 | p.Ser390Tyr | missense_variant | 0.14 |
ethA | 4326774 | p.Ala234Ser | missense_variant | 0.15 |
ethA | 4327950 | c.-477G>T | upstream_gene_variant | 0.2 |
ethA | 4328435 | c.-962C>A | upstream_gene_variant | 0.29 |
whiB6 | 4338260 | p.Arg88Trp | missense_variant | 1.0 |
whiB6 | 4338312 | c.210G>T | synonymous_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407620 | p.Tyr195His | missense_variant | 1.0 |
gid | 4407835 | p.Trp123Leu | missense_variant | 0.18 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408016 | p.Asp63Tyr | missense_variant | 0.13 |