Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49457791dupCA3847075MMUTc.656dup (p.Asn219LysfsTer2)
dbSNP ExAC gnomAD v2
6g.49457791delCA2499218333MMUTc.656del (p.Asn219MetfsTer4)
ClinVar dbSNP
6g.49457789T>ACA249731MMUTc.655A>T (p.Asn219Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457789T>CCA364404270MMUTc.655A>G (p.Asn219Asp)
6g.49457789T>GCA364404271MMUTc.655A>C (p.Asn219His)
6g.49457789T=CA1627392109MMUTc.655A= (p.Asn219=)
6g.49457790T>ACA364404272MMUTc.654A>T (p.Gln218His)
6g.49457790T>CCA450608788MMUTc.654A>G (p.Gln218=)
6g.49457790T>GCA364404273MMUTc.654A>C (p.Gln218His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49457790T=CA1627395125MMUTc.654A= (p.Gln218=)
6g.49457791T>ACA364404275MMUTc.653A>T (p.Gln218Leu)
6g.49457791T>CCA358798MMUTc.653A>G (p.Gln218Arg)
ClinVar dbSNP
6g.49457791T>GCA364404274MMUTc.653A>C (p.Gln218Pro)
6g.49457791T=CA1627395138MMUTc.653A= (p.Gln218=)
6g.49457792G>ACA3847076MMUTc.652C>T (p.Gln218Ter)
dbSNP ExAC gnomAD v2
6g.49457792G>CCA364404276MMUTc.652C>G (p.Gln218Glu)
ClinVar dbSNP
6g.49457792G=CA1627395151MMUTc.652C= (p.Gln218=)
6g.49457792G>TCA364404277MMUTc.652C>A (p.Gln218Lys)
6g.49457793G>ACA450608789MMUTc.651C>T (p.Ile217=)
dbSNP
6g.49457793G>CCA364404278MMUTc.651C>G (p.Ile217Met)
6g.49457793G=CA1627395162MMUTc.651C= (p.Ile217=)
6g.49457793G>TCA450608790MMUTc.651C>A (p.Ile217=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49457794A=CA1627395169MMUTc.650T= (p.Ile217=)
6g.49457794A>CCA364404279MMUTc.650T>G (p.Ile217Ser)
6g.49457794A>GCA364404280MMUTc.650T>C (p.Ile217Thr)
dbSNP gnomAD v2 gnomAD v4
6g.49457794A>TCA364404281MMUTc.650T>A (p.Ile217Asn)
6g.49457795T>ACA364404282MMUTc.649A>T (p.Ile217Phe)
6g.49457795T>CCA364404283MMUTc.649A>G (p.Ile217Val)
6g.49457795T>GCA364404284MMUTc.649A>C (p.Ile217Leu)
6g.49457796G>ACA3847077MMUTc.648C>T (p.Thr216=)
ClinVar dbSNP ExAC gnomAD v2
6g.49457796G>CCA450608791MMUTc.648C>G (p.Thr216=)
6g.49457796G=CA1627395171MMUTc.648C= (p.Thr216=)
6g.49457796G>TCA450608792MMUTc.648C>A (p.Thr216=)
6g.49457797G>ACA364404285MMUTc.647C>T (p.Thr216Ile)
6g.49457797G>CCA364404286MMUTc.647C>G (p.Thr216Ser)
6g.49457797G=CA1627395174MMUTc.647C= (p.Thr216=)
6g.49457797G>TCA364404287MMUTc.647C>A (p.Thr216Asn)
ClinVar dbSNP
6g.49457798T>ACA364404288MMUTc.646A>T (p.Thr216Ser)
6g.49457798T>CCA364404289MMUTc.646A>G (p.Thr216Ala)
6g.49457798T>GCA364404290MMUTc.646A>C (p.Thr216Pro)
6g.49457799A>CCA450608795MMUTc.645T>G (p.Gly215=)
6g.49457799A>GCA450608794MMUTc.645T>C (p.Gly215=)
ClinVar
6g.49457799A>TCA450608793MMUTc.645T>A (p.Gly215=)
6g.49457800C>ACA364404292MMUTc.644G>T (p.Gly215Val)
6g.49457800C=CA1627395179MMUTc.644G= (p.Gly215=)
6g.49457800C>GCA364404291MMUTc.644G>C (p.Gly215Ala)
6g.49457800C>TCA3847078MMUTc.644G>A (p.Gly215Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457801C>ACA16618294MMUTc.643G>T (p.Gly215Cys)
ClinVar dbSNP gnomAD v4
6g.49457801C=CA1627395185MMUTc.643G= (p.Gly215=)
6g.49457801C>GCA364404293MMUTc.643G>C (p.Gly215Arg)

Number of alleles fetched