GPRIN3[gene] and "single gene"[properties] - ClinVar

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Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282530	NM_198281.3(GPRIN3):c.2320G>C (p.Val774Leu)	GPRIN3 (V774L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102035	NM_198281.3(GPRIN3):c.2303G>C (p.Arg768Pro)	GPRIN3 (R768P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356895	NM_198281.3(GPRIN3):c.2299G>A (p.Val767Ile)	GPRIN3 (V767I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402685	NM_198281.3(GPRIN3):c.2287C>T (p.Pro763Ser)	GPRIN3 (P763S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542183	NM_198281.3(GPRIN3):c.2221T>G (p.Ser741Ala)	GPRIN3 (S741A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102034	NM_198281.3(GPRIN3):c.2212G>A (p.Asp738Asn)	GPRIN3 (D738N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460108	NM_198281.3(GPRIN3):c.2195G>A (p.Arg732Gln)	GPRIN3 (R732Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524118	NM_198281.3(GPRIN3):c.2185A>G (p.Ser729Gly)	GPRIN3 (S729G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2410147	NM_198281.3(GPRIN3):c.2107G>A (p.Glu703Lys)	GPRIN3 (E703K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523144	NM_198281.3(GPRIN3):c.2104G>A (p.Ala702Thr)	GPRIN3 (A702T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306745	NM_198281.3(GPRIN3):c.2104G>C (p.Ala702Pro)	GPRIN3 (A702P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2470182	NM_198281.3(GPRIN3):c.2038C>T (p.Arg680Cys)	GPRIN3 (R680C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589432	NM_198281.3(GPRIN3):c.2005G>T (p.Ala669Ser)	GPRIN3 (A669S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382815	NM_198281.3(GPRIN3):c.2005G>A (p.Ala669Thr)	GPRIN3 (A669T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545129	NM_198281.3(GPRIN3):c.1945G>A (p.Val649Met)	GPRIN3 (V649M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546339	NM_198281.3(GPRIN3):c.1918G>A (p.Glu640Lys)	GPRIN3 (E640K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102031	NM_198281.3(GPRIN3):c.1874C>G (p.Ser625Cys)	GPRIN3 (S625C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350608	NM_198281.3(GPRIN3):c.1838G>A (p.Gly613Asp)	GPRIN3 (G613D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282528	NM_198281.3(GPRIN3):c.1688T>C (p.Leu563Pro)	GPRIN3 (L563P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282524	NM_198281.3(GPRIN3):c.1637T>C (p.Val546Ala)	GPRIN3 (V546A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542943	NM_198281.3(GPRIN3):c.1616A>G (p.Lys539Arg)	GPRIN3 (K539R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241192	NM_198281.3(GPRIN3):c.1615A>C (p.Lys539Gln)	GPRIN3 (K539Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287171	NM_198281.3(GPRIN3):c.1600G>A (p.Asp534Asn)	GPRIN3 (D534N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102030	NM_198281.3(GPRIN3):c.1496C>T (p.Thr499Met)	GPRIN3 (T499M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454545	NM_198281.3(GPRIN3):c.1450G>A (p.Gly484Arg)	GPRIN3 (G484R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547937	NM_198281.3(GPRIN3):c.1367C>A (p.Ala456Glu)	GPRIN3 (A456E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612487	NM_198281.3(GPRIN3):c.1341G>T (p.Arg447Ser)	GPRIN3 (R447S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275203	NM_198281.3(GPRIN3):c.1294C>A (p.His432Asn)	GPRIN3 (H432N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102029	NM_198281.3(GPRIN3):c.1293G>T (p.Gln431His)	GPRIN3 (Q431H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379254	NM_198281.3(GPRIN3):c.1285A>G (p.Asn429Asp)	GPRIN3 (N429D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102028	NM_198281.3(GPRIN3):c.1235G>T (p.Ser412Ile)	GPRIN3 (S412I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588591	NM_198281.3(GPRIN3):c.1217G>C (p.Arg406Pro)	GPRIN3 (R406P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102026	NM_198281.3(GPRIN3):c.1192G>A (p.Ala398Thr)	GPRIN3 (A398T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368113	NM_198281.3(GPRIN3):c.1092C>A (p.Ser364Arg)	GPRIN3 (S364R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482913	NM_198281.3(GPRIN3):c.1042C>T (p.Arg348Cys)	GPRIN3 (R348C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790004	NM_198281.3(GPRIN3):c.1025C>A (p.Ala342Glu)	GPRIN3 (A342E)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2225999	NM_198281.3(GPRIN3):c.893C>G (p.Ala298Gly)	GPRIN3 (A298G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282527	NM_198281.3(GPRIN3):c.878C>T (p.Ser293Leu)	GPRIN3 (S293L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469543	NM_198281.3(GPRIN3):c.854C>T (p.Pro285Leu)	GPRIN3 (P285L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3102042	NM_198281.3(GPRIN3):c.833C>T (p.Pro278Leu)	GPRIN3 (P278L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375449	NM_198281.3(GPRIN3):c.820C>A (p.Pro274Thr)	GPRIN3 (P274T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528254	NM_198281.3(GPRIN3):c.680T>A (p.Ile227Asn)	GPRIN3 (I227N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102040	NM_198281.3(GPRIN3):c.646G>C (p.Val216Leu)	GPRIN3 (V216L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102039	NM_198281.3(GPRIN3):c.620G>A (p.Arg207Lys)	GPRIN3 (R207K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542776	NM_198281.3(GPRIN3):c.593C>T (p.Thr198Ile)	GPRIN3 (T198I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516902	NM_198281.3(GPRIN3):c.485C>T (p.Ser162Leu)	GPRIN3 (S162L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511582	NM_198281.3(GPRIN3):c.445T>A (p.Ser149Thr)	GPRIN3 (S149T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102038	NM_198281.3(GPRIN3):c.427C>T (p.Pro143Ser)	GPRIN3 (P143S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282525	NM_198281.3(GPRIN3):c.392A>G (p.Asn131Ser)	GPRIN3 (N131S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282529	NM_198281.3(GPRIN3):c.343T>G (p.Ser115Ala)	GPRIN3 (S115A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374335	NM_198281.3(GPRIN3):c.316A>G (p.Ser106Gly)	GPRIN3 (S106G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102037	NM_198281.3(GPRIN3):c.311G>C (p.Gly104Ala)	GPRIN3 (G104A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282523	NM_198281.3(GPRIN3):c.292G>A (p.Gly98Ser)	GPRIN3 (G98S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102036	NM_198281.3(GPRIN3):c.289C>T (p.Pro97Ser)	GPRIN3 (P97S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102032	NM_198281.3(GPRIN3):c.202G>T (p.Val68Phe)	GPRIN3 (V68F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235679	NM_198281.3(GPRIN3):c.202G>A (p.Val68Ile)	GPRIN3 (V68I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 56