Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.62020112C>TCA13336872ARID5Bc.733+19791C>T (n.733+19791C>T)
c.734-4561C>T (n.734-4561C>T)
c.503-30776C>T (n.503-30776C>T)
c.166+19791C>T (n.166+19791C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.62020112C=CA1914352064ARID5Bc.733+19791C= (n.733+19791C=)
c.734-4561C= (n.734-4561C=)
c.503-30776C= (n.503-30776C=)
c.166+19791C= (n.166+19791C=)
dbSNP

Number of alleles fetched