Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.17043907G>A | CA144284 | CUBN | c.3749C>T (p.Ser1250Phe) | ClinVar dbSNP |
10 | g.17043907G= | CA1893416250 | CUBN | c.3749C= (p.Ser1250=) | dbSNP |
10 | g.17043907G>C | CA376147787 | CUBN | c.3749C>G (p.Ser1250Cys) | dbSNP |