Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.61961417C>T | CA13156739 | ARID5B | c.502+21009C>T (n.502+21009C>T) c.-66+21009C>T (n.-66+21009C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.61961417C>G | CA208543709 | ARID5B | c.502+21009C>G (n.502+21009C>G) c.-66+21009C>G (n.-66+21009C>G) | dbSNP |