Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.17111045G>A | CA144305 | CUBN | c.889C>T (p.Gln297Ter) | ClinVar dbSNP gnomAD v4 |
10 | g.17111045G>C | CA376164774 | CUBN | c.889C>G (p.Gln297Glu) | dbSNP gnomAD v2 gnomAD v4 |
10 | g.17111045G>T | CA376164775 | CUBN | c.889C>A (p.Gln297Lys) | dbSNP gnomAD v4 |
10 | g.17111045G= | CA1893450305 | CUBN | c.889C= (p.Gln297=) | dbSNP |