| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.4299990T>C | CA6395342 | CCND2 | c.851T>C (p.Val284Ala) c.720+11000T>C (n.720+11000T>C) n.775T>C c.893T>C (p.Val298Ala) | ClinVar dbSNP ExAC gnomAD v2 |
| 12 | g.4299990T>G | CA10602706 | CCND2 | c.851T>G (p.Val284Gly) c.720+11000T>G (n.720+11000T>G) n.775T>G c.893T>G (p.Val298Gly) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.4299990T>A | CA383413803 | CCND2 | c.851T>A (p.Val284Glu) c.720+11000T>A (n.720+11000T>A) n.775T>A c.893T>A (p.Val298Glu) | ClinVar dbSNP COSMIC |
| 12 | g.4299990T= | CA2013096639 | CCND2 | c.851T= (p.Val284=) c.720+11000T= (n.720+11000T=) n.775T= c.893T= (p.Val298=) | dbSNP |