"PreventionGenetics, part of Exact Sciences"[submitter] AND "GRIA4"[ge - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3048830	NM_000829.4(GRIA4):c.52C>G (p.Leu18Val)	GRIA4, LOC129390350 (L18V)	Single nucleotide variant (missense variant +1 more)	GRIA4-related disorder	GLikely benign
Select item 2642332	NM_000829.4(GRIA4):c.312T>C (p.His104=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3057495	NM_000829.4(GRIA4):c.411G>A (p.Ser137=)	GRIA4, LOC126861324	Single nucleotide variant (synonymous variant +1 more)	GRIA4-related disorder	GLikely benign
Select item 3055393	NM_000829.4(GRIA4):c.886-7T>C	GRIA4	Single nucleotide variant (intron variant)	GRIA4-related disorder	GBenign
Select item 2629800	NM_000829.4(GRIA4):c.1186T>G (p.Leu396Val)	GRIA4 (L396V)	Single nucleotide variant (missense variant +1 more)	GRIA4-related disorder	GUncertain significance
Select item 3035877	NM_000829.4(GRIA4):c.1326G>A (p.Lys442=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	GRIA4-related disorder	GLikely benign
Select item 2633052	NM_000829.4(GRIA4):c.1370A>T (p.His457Leu)	GRIA4 (H457L)	Single nucleotide variant (missense variant +1 more)	GRIA4-related disorder	GUncertain significance
Select item 2631197	NM_000829.4(GRIA4):c.1378A>G (p.Ile460Val)	GRIA4 (I460V)	Single nucleotide variant (missense variant +1 more)	GRIA4-related disorder	GUncertain significance
Select item 2630432	NM_000829.4(GRIA4):c.1667T>C (p.Ile556Thr)	GRIA4 (I556T)	Single nucleotide variant (missense variant +1 more)	GRIA4-related disorder	GUncertain significance
Select item 2642339	NM_000829.4(GRIA4):c.1812T>G (p.Gly604=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2631231	NM_000829.4(GRIA4):c.2099A>G (p.Glu700Gly)	GRIA4 (E700G)	Single nucleotide variant (missense variant +1 more)	GRIA4-related disorder	GUncertain significance
Select item 2642344	NM_000829.4(GRIA4):c.2532G>A (p.Ala844=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 974624	NM_000829.4(GRIA4):c.2615G>A (p.Arg872His)	GRIA4 (R872H)	Single nucleotide variant (missense variant +2 more)	GRIA4-related disorder +2 more	GConflicting classifications of pathogenicity