Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.43120185C>A | CA040485 | RET | c.2316C>A (p.Ser772=) n.2286C>A n.2277C>A c.2712C>A (p.Ser904=) c.*1306C>A (n.*1306C>A) c.*61C>A (n.*61C>A) c.1950C>A (p.Ser650=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.43120185C>G | CA009034 | RET | c.2316C>G (p.Ser772=) n.2286C>G n.2277C>G c.2712C>G (p.Ser904=) c.*1306C>G (n.*1306C>G) c.*61C>G (n.*61C>G) c.1950C>G (p.Ser650=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.43120185C>T | CA469029015 | RET | c.2316C>T (p.Ser772=) n.2286C>T n.2277C>T c.2712C>T (p.Ser904=) c.*1306C>T (n.*1306C>T) c.*61C>T (n.*61C>T) c.1950C>T (p.Ser650=) | dbSNP |