KIF3C[gene] and "single gene"[properties] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2348109	NM_002254.8(KIF3C):c.2354G>A (p.Arg785His)	KIF3C (R785H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3114907	NM_002254.8(KIF3C):c.2353C>T (p.Arg785Cys)	KIF3C (R785C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114905	NM_002254.8(KIF3C):c.2336T>C (p.Leu779Pro)	KIF3C (L779P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454305	NM_002254.8(KIF3C):c.2333C>G (p.Ser778Cys)	KIF3C (S778C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288630	NM_002254.8(KIF3C):c.2273G>A (p.Arg758Gln)	KIF3C (R758Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114904	NM_002254.8(KIF3C):c.2238C>G (p.Asp746Glu)	KIF3C (D746E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602323	NM_002254.8(KIF3C):c.2129T>C (p.Met710Thr)	KIF3C (M710T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485694	NM_002254.8(KIF3C):c.2022G>A (p.Met674Ile)	KIF3C (M674I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524636	NM_002254.8(KIF3C):c.1973A>G (p.Gln658Arg)	KIF3C (Q658R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554336	NM_002254.8(KIF3C):c.1921G>C (p.Glu641Gln)	KIF3C (E641Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478951	NM_002254.8(KIF3C):c.1888A>C (p.Lys630Gln)	KIF3C (K630Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114903	NM_002254.8(KIF3C):c.1702A>G (p.Met568Val)	KIF3C (M568V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114902	NM_002254.8(KIF3C):c.1687C>T (p.Arg563Trp)	KIF3C (R563W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114901	NM_002254.8(KIF3C):c.1670A>G (p.Gln557Arg)	KIF3C (Q557R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334248	NM_002254.8(KIF3C):c.1666A>T (p.Met556Leu)	KIF3C (M556L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496262	NM_002254.8(KIF3C):c.1655G>A (p.Arg552His)	KIF3C (R552H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247692	NM_002254.8(KIF3C):c.1586T>C (p.Met529Thr)	KIF3C (M529T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114900	NM_002254.8(KIF3C):c.1505G>A (p.Arg502Gln)	KIF3C (R502Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371201	NM_002254.8(KIF3C):c.1486A>C (p.Met496Leu)	KIF3C (M496L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288629	NM_002254.8(KIF3C):c.1415A>C (p.Lys472Thr)	KIF3C (K472T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114899	NM_002254.8(KIF3C):c.1284G>C (p.Glu428Asp)	KIF3C (E428D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454443	NM_002254.8(KIF3C):c.1214G>A (p.Arg405Gln)	KIF3C (R405Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369322	NM_002254.8(KIF3C):c.1151A>G (p.Gln384Arg)	KIF3C (Q384R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114911	NM_002254.8(KIF3C):c.991G>C (p.Gly331Arg)	KIF3C (G331R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114910	NM_002254.8(KIF3C):c.815G>A (p.Gly272Asp)	KIF3C (G272D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288631	NM_002254.8(KIF3C):c.814G>A (p.Gly272Ser)	KIF3C (G272S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2293957	NM_002254.8(KIF3C):c.782C>A (p.Ala261Glu)	KIF3C (A261E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2637951	NM_002254.8(KIF3C):c.712C>T (p.Arg238Ter)	KIF3C (R238*)	Single nucleotide variant (nonsense)	KIF3C-related neurodevelopmental disorder	GUncertain significance
Select item 2303979	NM_002254.8(KIF3C):c.613G>A (p.Gly205Ser)	KIF3C (G205S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114909	NM_002254.8(KIF3C):c.482C>T (p.Pro161Leu)	KIF3C (P161L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390073	NM_002254.8(KIF3C):c.425G>A (p.Arg142Gln)	KIF3C (R142Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114908	NM_002254.8(KIF3C):c.418C>A (p.Leu140Met)	KIF3C (L140M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539596	NM_002254.8(KIF3C):c.164C>T (p.Pro55Leu)	KIF3C (P55L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 33