Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.6770442G>ACA9758643BMP2c.316G>A (p.Ala106Thr)
c.-123+1567G>A (n.-123+1567G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.6770442G>CCA408260674BMP2c.316G>C (p.Ala106Pro)
c.-123+1567G>C (n.-123+1567G>C)
20g.6770442G=CA2348108711BMP2c.316G= (p.Ala106=)
c.-123+1567G= (n.-123+1567G=)
20g.6770442G>TCA408260675BMP2c.316G>T (p.Ala106Ser)
c.-123+1567G>T (n.-123+1567G>T)
20g.6770443C>ACA408260676BMP2c.317C>A (p.Ala106Asp)
c.-123+1568C>A (n.-123+1568C>A)
gnomAD v4
20g.6770443C>GCA408260677BMP2c.317C>G (p.Ala106Gly)
c.-123+1568C>G (n.-123+1568C>G)
20g.6770443C>TCA408260678BMP2c.317C>T (p.Ala106Val)
c.-123+1568C>T (n.-123+1568C>T)
20g.6770444C>ACA509817981BMP2c.318C>A (p.Ala106=)
c.-123+1569C>A (n.-123+1569C>A)
20g.6770444C=CA2348108712BMP2c.318C= (p.Ala106=)
c.-123+1569C= (n.-123+1569C=)
20g.6770444C>GCA509817979BMP2c.318C>G (p.Ala106=)
c.-123+1569C>G (n.-123+1569C>G)
dbSNP gnomAD v2
20g.6770444C>TCA509817978BMP2c.318C>T (p.Ala106=)
c.-123+1569C>T (n.-123+1569C>T)
20g.6770445A=CA2348108713BMP2c.319A= (p.Asn107=)
c.-123+1570A= (n.-123+1570A=)
20g.6770445A>CCA408260679BMP2c.319A>C (p.Asn107His)
c.-123+1570A>C (n.-123+1570A>C)
20g.6770445A>GCA311471120BMP2c.319A>G (p.Asn107Asp)
c.-123+1570A>G (n.-123+1570A>G)
dbSNP
20g.6770445A>TCA408260680BMP2c.319A>T (p.Asn107Tyr)
c.-123+1570A>T (n.-123+1570A>T)
20g.6770446A>CCA408260683BMP2c.320A>C (p.Asn107Thr)
c.-123+1571A>C (n.-123+1571A>C)
20g.6770446A>GCA408260681BMP2c.320A>G (p.Asn107Ser)
c.-123+1571A>G (n.-123+1571A>G)
20g.6770446A>TCA408260682BMP2c.320A>T (p.Asn107Ile)
c.-123+1571A>T (n.-123+1571A>T)
20g.6770447C>ACA408260684BMP2c.321C>A (p.Asn107Lys)
c.-123+1572C>A (n.-123+1572C>A)
20g.6770447C>GCA408260685BMP2c.321C>G (p.Asn107Lys)
c.-123+1572C>G (n.-123+1572C>G)
20g.6770447C>TCA509817986BMP2c.321C>T (p.Asn107=)
c.-123+1572C>T (n.-123+1572C>T)
20g.6770448A>CCA408260686BMP2c.322A>C (p.Thr108Pro)
c.-123+1573A>C (n.-123+1573A>C)
20g.6770448A>GCA408260687BMP2c.322A>G (p.Thr108Ala)
c.-123+1573A>G (n.-123+1573A>G)
20g.6770448A>TCA408260688BMP2c.322A>T (p.Thr108Ser)
c.-123+1573A>T (n.-123+1573A>T)
20g.6770449C>ACA408260689BMP2c.323C>A (p.Thr108Asn)
c.-123+1574C>A (n.-123+1574C>A)
gnomAD v4
20g.6770449C=CA2348108714BMP2c.323C= (p.Thr108=)
c.-123+1574C= (n.-123+1574C=)
20g.6770449C>GCA408260690BMP2c.323C>G (p.Thr108Ser)
c.-123+1574C>G (n.-123+1574C>G)
gnomAD v4
20g.6770449C>TCA9758644BMP2c.323C>T (p.Thr108Ile)
c.-123+1574C>T (n.-123+1574C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.6770450T>ACA509817987BMP2c.324T>A (p.Thr108=)
c.-123+1575T>A (n.-123+1575T>A)
20g.6770450T>CCA509817989BMP2c.324T>C (p.Thr108=)
c.-123+1575T>C (n.-123+1575T>C)
20g.6770450T>GCA509817988BMP2c.324T>G (p.Thr108=)
c.-123+1575T>G (n.-123+1575T>G)
20g.6770451G>ACA408260691BMP2c.325G>A (p.Val109Met)
c.-123+1576G>A (n.-123+1576G>A)
dbSNP gnomAD v2
20g.6770451G>CCA408260692BMP2c.325G>C (p.Val109Leu)
c.-123+1576G>C (n.-123+1576G>C)
20g.6770451G=CA2348108715BMP2c.325G= (p.Val109=)
c.-123+1576G= (n.-123+1576G=)
20g.6770451G>TCA408260693BMP2c.325G>T (p.Val109Leu)
c.-123+1576G>T (n.-123+1576G>T)
20g.6770452delCA2740097004BMP2c.326del (p.Val109GlyfsTer28)
c.-123+1577del (n.-123+1577del)
ClinVar
20g.6770452T>ACA408260695BMP2c.326T>A (p.Val109Glu)
c.-123+1577T>A (n.-123+1577T>A)
20g.6770452T>CCA9758645BMP2c.326T>C (p.Val109Ala)
c.-123+1577T>C (n.-123+1577T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.6770452T>GCA408260694BMP2c.326T>G (p.Val109Gly)
c.-123+1577T>G (n.-123+1577T>G)
20g.6770452T=CA2348108716BMP2c.326T= (p.Val109=)
c.-123+1577T= (n.-123+1577T=)
20g.6770453G>ACA509817991BMP2c.327G>A (p.Val109=)
c.-123+1578G>A (n.-123+1578G>A)
dbSNP gnomAD v4
20g.6770453G>CCA509817993BMP2c.327G>C (p.Val109=)
c.-123+1578G>C (n.-123+1578G>C)
20g.6770453G=CA2348108717BMP2c.327G= (p.Val109=)
c.-123+1578G= (n.-123+1578G=)
20g.6770453G>TCA509817994BMP2c.327G>T (p.Val109=)
c.-123+1578G>T (n.-123+1578G>T)
20g.6770454C>ACA408260696BMP2c.328C>A (p.Arg110Ser)
c.-123+1579C>A (n.-123+1579C>A)
gnomAD v4
20g.6770454C>GCA408260698BMP2c.328C>G (p.Arg110Gly)
c.-123+1579C>G (n.-123+1579C>G)
20g.6770454C>TCA408260697BMP2c.328C>T (p.Arg110Cys)
c.-123+1579C>T (n.-123+1579C>T)
20g.6770455G>ACA408260699BMP2c.329G>A (p.Arg110His)
c.-123+1580G>A (n.-123+1580G>A)
ClinVar dbSNP gnomAD v4
20g.6770455G>CCA408260700BMP2c.329G>C (p.Arg110Pro)
c.-123+1580G>C (n.-123+1580G>C)
20g.6770455G>TCA408260701BMP2c.329G>T (p.Arg110Leu)
c.-123+1580G>T (n.-123+1580G>T)

Number of alleles fetched