Related gene-specific medical variations for Gene (Select 100507470) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689160	NM_017551.3(GRID1):c.2636G>A (p.Arg879His)	GRID1, GRID1-AS1 (R879H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2590488	NM_017551.3(GRID1):c.2939C>T (p.Pro980Leu)	GRID1, GRID1-AS1 (P980L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561444	NM_017551.3(GRID1):c.2753G>A (p.Arg918Gln)	GRID1, GRID1-AS1 (R918Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2502410	NM_017551.3(GRID1):c.2950C>T (p.Pro984Ser)	GRID1, GRID1-AS1 (P984S)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2502409	NM_017551.3(GRID1):c.2855C>T (p.Pro952Leu)	GRID1, GRID1-AS1 (P952L)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2502408	NM_017551.3(GRID1):c.2690C>T (p.Ser897Leu)	GRID1, GRID1-AS1 (S897L)	Single nucleotide variant (missense variant)	GRID1-associated neurodevelopmental disorder	GUncertain significance
Select item 2207898	NM_017551.3(GRID1):c.2984G>A (p.Gly995Asp)	GRID1, GRID1-AS1 (G995D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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