Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.40300899G>C | CA8542116 | CDC6 | c.1321G>C (p.Val441Leu) n.10G>C c.1441G>C (p.Val481Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.40300899G>A | CA152214 | CDC6 | c.1321G>A (p.Val441Ile) n.10G>A c.1441G>A (p.Val481Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.40300899G>T | CA399335266 | CDC6 | c.1321G>T (p.Val441Phe) n.10G>T c.1441G>T (p.Val481Phe) | dbSNP |