Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.17114152A>G | CA5425509 | CUBN | c.758T>C (p.Phe253Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.17114152A>C | CA376165673 | CUBN | c.758T>G (p.Phe253Cys) | dbSNP |
10 | g.17114152A>T | CA376165674 | CUBN | c.758T>A (p.Phe253Tyr) | dbSNP |
10 | g.17114152A= | CA1893453254 | CUBN | c.758T= (p.Phe253=) | dbSNP |