Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.61950345A>C | CA1914321684 | ARID5B | c.502+9937A>C (n.502+9937A>C) c.-66+9937A>C (n.-66+9937A>C) | dbSNP |
10 | g.61950345A>G | CA13156736 | ARID5B | c.502+9937A>G (n.502+9937A>G) c.-66+9937A>G (n.-66+9937A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |