Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.218891661C>T | CA11098263 | WNT10A | c.757-1113C>T (n.757-1113C>T) c.264-1113C>T c.706-1113C>T (n.706-1113C>T) c.661-1113C>T (n.661-1113C>T) c.377-1113C>T (n.377-1113C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218891661C>G | CA764942717 | WNT10A | c.757-1113C>G (n.757-1113C>G) c.264-1113C>G c.706-1113C>G (n.706-1113C>G) c.661-1113C>G (n.661-1113C>G) c.377-1113C>G (n.377-1113C>G) | dbSNP gnomAD v3 gnomAD v4 |