Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.111119021A>GCA115071WDR36c.1805A>G (p.Asp602Gly)
c.1973A>G (p.Asp658Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.111119021A>TCA360613446WDR36c.1805A>T (p.Asp602Val)
c.1973A>T (p.Asp658Val)
dbSNP
5g.111119021A=CA1572628322WDR36c.1805A= (p.Asp602=)
c.1973A= (p.Asp658=)
dbSNP

Number of alleles fetched