Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.151672371C>ACA348816362NEBc.4297G>T (p.Asp1433Tyr)
2g.151672371C>GCA348816363NEBc.4297G>C (p.Asp1433His)
2g.151672371C>TCA348816364NEBc.4297G>A (p.Asp1433Asn)
2g.151672372A>CCA348816365NEBc.4296T>G (p.Ser1432Arg)
2g.151672372A>GCA429453378NEBc.4296T>C (p.Ser1432=)
gnomAD v4
2g.151672372A>TCA348816366NEBc.4296T>A (p.Ser1432Arg)
2g.151672373C>ACA348816367NEBc.4295G>T (p.Ser1432Ile)
2g.151672373C=CA1298290943NEBc.4295G= (p.Ser1432=)
2g.151672373C>GCA348816368NEBc.4295G>C (p.Ser1432Thr)
2g.151672373C>TCA1910683NEBc.4295G>A (p.Ser1432Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.151672374T>ACA348816369NEBc.4294A>T (p.Ser1432Cys)
2g.151672374T>CCA348816370NEBc.4294A>G (p.Ser1432Gly)
2g.151672374T>GCA348816371NEBc.4294A>C (p.Ser1432Arg)
2g.151672375C>ACA348816372NEBc.4293G>T (p.Gln1431His)
2g.151672375C>GCA348816373NEBc.4293G>C (p.Gln1431His)
2g.151672375C>TCA429453379NEBc.4293G>A (p.Gln1431=)
COSMIC COSMIC COSMIC
2g.151672376T>ACA348816374NEBc.4292A>T (p.Gln1431Leu)
2g.151672376T>CCA348816376NEBc.4292A>G (p.Gln1431Arg)
gnomAD v4
2g.151672376T>GCA348816375NEBc.4292A>C (p.Gln1431Pro)
2g.151672377G>ACA348816377NEBc.4291C>T (p.Gln1431Ter)
2g.151672377G>CCA348816378NEBc.4291C>G (p.Gln1431Glu)
2g.151672377G>TCA348816379NEBc.4291C>A (p.Gln1431Lys)
2g.151672378A>CCA348816380NEBc.4290T>G (p.Ile1430Met)
2g.151672378A>GCA429453381NEBc.4290T>C (p.Ile1430=)
2g.151672378A>TCA429453380NEBc.4290T>A (p.Ile1430=)
2g.151672379A=CA1298290945NEBc.4289T= (p.Ile1430=)
2g.151672379A>CCA348816381NEBc.4289T>G (p.Ile1430Ser)
2g.151672379A>GCA348816382NEBc.4289T>C (p.Ile1430Thr)
2g.151672379A>TCA1910684NEBc.4289T>A (p.Ile1430Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.151672380T>ACA348816383NEBc.4288A>T (p.Ile1430Phe)
2g.151672380T>CCA348816384NEBc.4288A>G (p.Ile1430Val)
2g.151672380T>GCA348816385NEBc.4288A>C (p.Ile1430Leu)
2g.151672381T>ACA348816386NEBc.4287A>T (p.Gln1429His)
2g.151672381T>CCA429453382NEBc.4287A>G (p.Gln1429=)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.151672381T>GCA348816387NEBc.4287A>C (p.Gln1429His)
2g.151672381T=CA1298290948NEBc.4287A= (p.Gln1429=)
2g.151672382T>ACA348816390NEBc.4286A>T (p.Gln1429Leu)
2g.151672382T>CCA348816388NEBc.4286A>G (p.Gln1429Arg)
2g.151672382T>GCA348816389NEBc.4286A>C (p.Gln1429Pro)
2g.151672383G>ACA348816391NEBc.4285C>T (p.Gln1429Ter)
2g.151672383G>CCA348816392NEBc.4285C>G (p.Gln1429Glu)
2g.151672383G>TCA348816393NEBc.4285C>A (p.Gln1429Lys)
2g.151672384A>CCA348816394NEBc.4284T>G (p.Asn1428Lys)
2g.151672384A>GCA429453383NEBc.4284T>C (p.Asn1428=)
ClinVar dbSNP
2g.151672384A>TCA348816395NEBc.4284T>A (p.Asn1428Lys)
2g.151672385T>ACA348816396NEBc.4283A>T (p.Asn1428Ile)
2g.151672385T>CCA1910685NEBc.4283A>G (p.Asn1428Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.151672385T>GCA348816397NEBc.4283A>C (p.Asn1428Thr)
2g.151672385T=CA1298290953NEBc.4283A= (p.Asn1428=)
2g.151672386T>ACA348816398NEBc.4282A>T (p.Asn1428Tyr)

Number of alleles fetched