"Ambry Genetics"[submitter] AND "GRM8"[gene] - ClinVar

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Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2592522	NM_000845.3(GRM8):c.2677+18T>C	GRM8 (F899L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2461942	NM_000845.3(GRM8):c.2555G>A (p.Arg852His)	GRM8 (R852H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304474	NM_000845.3(GRM8):c.2510A>G (p.Lys837Arg)	GRM8 (K837R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232870	NM_000845.3(GRM8):c.2452C>A (p.Leu818Ile)	GRM8 (L818I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227644	NM_000845.3(GRM8):c.2432T>G (p.Met811Arg)	GRM8 (M811R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102713	NM_000845.3(GRM8):c.2309C>T (p.Thr770Met)	GRM8 (T770M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331871	NM_000845.3(GRM8):c.2272C>T (p.Leu758Phe)	GRM8 (L758F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282908	NM_000845.3(GRM8):c.2163C>G (p.Ile721Met)	GRM8 (I721M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401589	NM_000845.3(GRM8):c.2158C>T (p.His720Tyr)	GRM8 (H515Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270025	NM_000845.3(GRM8):c.1955G>A (p.Arg652Gln)	GRM8 (R447Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481035	NM_000845.3(GRM8):c.1952G>A (p.Arg651Gln)	GRM8 (R651Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102712	NM_000845.3(GRM8):c.1915A>G (p.Met639Val)	GRM8 (M434V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384852	NM_000845.3(GRM8):c.1880C>T (p.Thr627Met)	GRM8 (T627M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205971	NM_000845.3(GRM8):c.1870G>A (p.Val624Met)	GRM8 (V624M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316566	NM_000845.3(GRM8):c.1852G>A (p.Gly618Arg)	GRM8 (G618R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102711	NM_000845.3(GRM8):c.1839C>G (p.Ile613Met)	GRM8 (I613M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553923	NM_000845.3(GRM8):c.1819C>T (p.Arg607Cys)	GRM8 (R402C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102710	NM_000845.3(GRM8):c.1813T>C (p.Phe605Leu)	GRM8 (F400L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340998	NM_000845.3(GRM8):c.1796C>T (p.Thr599Ile)	GRM8 (T394I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102709	NM_000845.3(GRM8):c.1697G>A (p.Arg566His)	GRM8 (R361H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358768	NM_000845.3(GRM8):c.1635C>A (p.Asn545Lys)	GRM8 (N545K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2568443	NM_000845.3(GRM8):c.1628G>A (p.Gly543Asp)	GRM8 (G543D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522852	NM_000845.3(GRM8):c.1618C>T (p.Arg540Cys)	GRM8 (R335C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554068	NM_000845.3(GRM8):c.1556C>T (p.Pro519Leu)	GRM8 (P314L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102708	NM_000845.3(GRM8):c.1510T>C (p.Trp504Arg)	GRM8 (W299R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102707	NM_000845.3(GRM8):c.1339C>T (p.Arg447Trp)	GRM8 (R242W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102706	NM_000845.3(GRM8):c.1315G>A (p.Gly439Arg)	GRM8 (G234R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102705	NM_000845.3(GRM8):c.1255A>G (p.Met419Val)	GRM8 (M214V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102704	NM_000845.3(GRM8):c.1231T>A (p.Ser411Thr)	GRM8 (S411T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282907	NM_000845.3(GRM8):c.1141A>G (p.Ile381Val)	GRM8 (I176V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314857	NM_000845.3(GRM8):c.1057A>G (p.Asn353Asp)	GRM8 (N148D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454243	NM_000845.3(GRM8):c.959A>T (p.Gln320Leu)	GRM8 (Q115L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487217	NM_000845.3(GRM8):c.839T>C (p.Met280Thr)	GRM8 (M75T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611630	NM_000845.3(GRM8):c.773G>A (p.Arg258Lys)	GRM8 (R258K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479307	NM_000845.3(GRM8):c.640G>C (p.Gly214Arg)	GRM8 (G214R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256146	NM_000845.3(GRM8):c.538G>T (p.Ala180Ser)	GRM8 (A180S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102715	NM_000845.3(GRM8):c.482T>C (p.Met161Thr)	GRM8 (M161T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2621940	NM_000845.3(GRM8):c.472G>A (p.Val158Met)	GRM8 (V158M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102714	NM_000845.3(GRM8):c.445G>T (p.Gly149Cys)	GRM8 (G149C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2219598	NM_000845.3(GRM8):c.433G>A (p.Asp145Asn)	GRM8 (D145N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2589829	NM_000845.3(GRM8):c.406G>A (p.Gly136Arg)	GRM8 (G136R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2382116	NM_000845.3(GRM8):c.390T>G (p.Asp130Glu)	GRM8 (D130E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2466915	NM_000845.3(GRM8):c.358G>A (p.Val120Met)	GRM8 (V120M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2621578	NM_000845.3(GRM8):c.343C>A (p.Gln115Lys)	GRM8 (Q115K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2336044	NM_000845.3(GRM8):c.329C>T (p.Thr110Ile)	GRM8 (T110I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2255380	NM_000845.3(GRM8):c.182G>A (p.Gly61Glu)	GRM8 (G61E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2531025	NM_000845.3(GRM8):c.53C>A (p.Thr18Asn)	GRM8 (T18N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2310543	NM_000845.3(GRM8):c.26C>G (p.Ala9Gly)	GRM8 (A9G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2547660	NM_000845.3(GRM8):c.20G>T (p.Arg7Leu)	GRM8 (R7L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2358397	NM_000845.3(GRM8):c.20G>A (p.Arg7Gln)	GRM8 (R7Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 50