"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "GRIA4"[gen - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1335083	NM_000829.4(GRIA4):c.166A>C (p.Asn56His)	GRIA4 (N56H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
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 781814	NM_000829.4(GRIA4):c.436C>T (p.Leu146=)	GRIA4, LOC126861324	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2642333	NM_000829.4(GRIA4):c.487+44507A>C	GRIA4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2642334	NM_000829.4(GRIA4):c.487+44641A>G	GRIA4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1694645	NM_000829.4(GRIA4):c.573T>G (p.Asp191Glu)	GRIA4 (D191E)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2642335	NM_000829.4(GRIA4):c.662T>C (p.Ile221Thr)	GRIA4 (I221T)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2642336	NM_000829.4(GRIA4):c.708T>C (p.His236=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3067334	NM_000829.4(GRIA4):c.790T>C (p.Leu264=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3067241	NM_000829.4(GRIA4):c.817A>C (p.Ile273Leu)	GRIA4 (I273L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3027092	NM_000829.4(GRIA4):c.949A>T (p.Arg317Trp)	GRIA4 (R317W)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1694646	NM_000829.4(GRIA4):c.1216G>C (p.Gly406Arg)	GRIA4 (G406R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1012994	NM_000829.4(GRIA4):c.1234A>G (p.Ile412Val)	GRIA4 (I412V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1298525	NM_000829.4(GRIA4):c.1416T>C (p.Tyr472=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642337	NM_000829.4(GRIA4):c.1431A>C (p.Ala477=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642338	NM_000829.4(GRIA4):c.1433A>C (p.Asp478Ala)	GRIA4 (D478A)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3026398	NM_000829.4(GRIA4):c.1735G>A (p.Glu579Lys)	GRIA4 (E579K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2368808	NM_000829.4(GRIA4):c.1738G>A (p.Asp580Asn)	GRIA4 (D580N)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2642339	NM_000829.4(GRIA4):c.1812T>G (p.Gly604=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	GRIA4-related condition +1 more	GLikely benign
Select item 2498531	NM_000829.4(GRIA4):c.1903A>G (p.Ile635Val)	GRIA4 (I635V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2642340	NM_000829.4(GRIA4):c.2127T>C (p.Ala709=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642341	NM_000829.4(GRIA4):c.2226G>T (p.Thr742=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3026988	NM_000829.4(GRIA4):c.2295-5891G>A	GRIA4 (D791N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 779265	NM_000829.4(GRIA4):c.2410-5C>A	GRIA4	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 2642342	NM_000829.4(GRIA4):c.2421T>C (p.Ser807=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1701176	NM_000829.4(GRIA4):c.2448C>T (p.Gly816=)	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3026141	NM_000829.4(GRIA4):c.2449G>A (p.Val817Ile)	GRIA4 (V817I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2642343	NM_000829.4(GRIA4):c.2531C>T (p.Ala844Val)	GRIA4 (A844V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
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 2642345	NM_000829.4(GRIA4):c.2544+93C>T	GRIA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642346	NM_000829.4(GRIA4):c.2688C>G (p.Val896=)	GRIA4	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3026687	NM_000829.4(GRIA4):c.2708A>G (p.Ter903=)	GRIA4	Single nucleotide variant (synonymous variant +2 more)	not provided	GUncertain significance

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Items: 32