| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.67753950G>C | CA2938949 | GNRHR | c.386C>G (p.Ala129Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.67753950G>T | CA130203 | GNRHR | c.386C>A (p.Ala129Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.67753950G>A | CA357054682 | GNRHR | c.386C>T (p.Ala129Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |