Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.162778617G>C | CA343417024 | DDR2 | c.2321G>C (p.Gly774Ala) | dbSNP |
1 | g.162778617G>A | CA343417023 | DDR2 | c.2321G>A (p.Gly774Glu) | dbSNP |
1 | g.162778617G>T | CA16602601 | DDR2 | c.2321G>T (p.Gly774Val) | ClinVar dbSNP |