Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.240603286C>T | CA11284546 | CAPN10 | c.274-13102C>T (n.274-13102C>T) c.167-3101C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240603286C>G | CA766892664 | CAPN10 | c.274-13102C>G (n.274-13102C>G) c.167-3101C>G | dbSNP |