Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13488772C>G | CA685664009 | GRIN2B | c.70-50761G>C (n.70-50761G>C) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.13488772C>A | CA233118256 | GRIN2B | c.70-50761G>T (n.70-50761G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13488772C= | CA2017411472 | GRIN2B | c.70-50761G= (n.70-50761G=) | dbSNP |