Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.69651969C>G | CA13386459 | CCND1 | c.*687C>G (n.*687C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69651969C>T | CA679685000 | CCND1 | c.*687C>T (n.*687C>T) | dbSNP gnomAD v4 |
11 | g.69651969C>A | CA2581028408 | CCND1 | c.*687C>A (n.*687C>A) | dbSNP |