"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "GRIN1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 568144	NM_007327.4(GRIN1):c.1012G>A (p.Val338Met)	GRIN1 (V338M +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1057556	NM_007327.4(GRIN1):c.1339C>T (p.Pro447Ser)	GRIN1 (P447S +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 8 +1 more	GUncertain significance
Select item 1163324	NM_007327.4(GRIN1):c.2021A>T (p.Asn674Ile)	GRIN1 (N674I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 388106	NM_007327.4(GRIN1):c.2589+6G>T	GRIN1	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 8 +1 more	GConflicting classifications of pathogenicity
Select item 1120164	Single allele	GRIN1	Duplication	not provided	GUncertain significance
Select item 1120163	Single allele	GRIN1	Duplication	not provided	GUncertain significance

ClinVar