Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.67753920C>T | CA249862 | GNRHR | c.416G>A (p.Arg139His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.67753920C= | CA1465420612 | GNRHR | c.416G= (p.Arg139=) | dbSNP |
4 | g.67753920C>A | CA357054555 | GNRHR | c.416G>T (p.Arg139Leu) | ClinVar dbSNP |
4 | g.67753920C>G | CA357054557 | GNRHR | c.416G>C (p.Arg139Pro) | dbSNP gnomAD v4 |