| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.67737817C>A | CA10618143 | GNRHR | c.*2663G>T (n.*2663G>T) c.*2772G>T (n.*2772G>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.67737817C>T | CA98666702 | GNRHR | c.*2663G>A (n.*2663G>A) c.*2772G>A (n.*2772G>A) | dbSNP gnomAD v3 gnomAD v4 |