Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.23523239C>G | CA1533066414 | PRDM9 | c.883-52C>G (n.883-52C>G) c.706-52C>G (n.706-52C>G) | dbSNP |
5 | g.23523239C>T | CA11997353 | PRDM9 | c.883-52C>T (n.883-52C>T) c.706-52C>T (n.706-52C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |