Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.62020112C>T | CA13336872 | ARID5B | c.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 |
10 | g.62020112C= | CA1914352064 | ARID5B | c.733+19791C= (n.733+19791C=) c.734-4561C= (n.734-4561C=) c.503-30776C= (n.503-30776C=) c.166+19791C= (n.166+19791C=) | dbSNP |