FNIP2[gene] and "single gene"[properties] - ClinVar

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Items: 69

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2525317	NM_020840.3(FNIP2):c.65C>T (p.Ala22Val)	FNIP2 (A22V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2333625	NM_020840.3(FNIP2):c.112T>C (p.Ser38Pro)	FNIP2 (S38P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279446	NM_020840.3(FNIP2):c.287G>A (p.Ser96Asn)	FNIP2 (S119N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096152	NM_020840.3(FNIP2):c.395C>T (p.Ala132Val)	FNIP2 (A132V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286061	NM_020840.3(FNIP2):c.634T>C (p.Cys212Arg)	FNIP2 (C212R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515241	NM_020840.3(FNIP2):c.785C>G (p.Ser262Cys)	FNIP2 (S262C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096153	NM_020840.3(FNIP2):c.891A>T (p.Glu297Asp)	FNIP2 (E350D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279439	NM_020840.3(FNIP2):c.937A>G (p.Ile313Val)	FNIP2 (I336V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554870	NM_020840.3(FNIP2):c.941G>A (p.Ser314Asn)	FNIP2 (S337N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312043	NM_020840.3(FNIP2):c.994T>G (p.Phe332Val)	FNIP2 (F355V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312044	NM_020840.3(FNIP2):c.995T>A (p.Phe332Tyr)	FNIP2 (F385Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294275	NM_020840.3(FNIP2):c.1037G>A (p.Arg346Lys)	FNIP2 (R369K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282167	NM_020840.3(FNIP2):c.1121G>A (p.Arg374His)	FNIP2 (R20H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302692	NM_020840.3(FNIP2):c.1168T>C (p.Tyr390His)	FNIP2 (Y443H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221356	NM_020840.3(FNIP2):c.1255A>G (p.Lys419Glu)	FNIP2 (K419E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231944	NM_020840.3(FNIP2):c.1275A>G (p.Ile425Met)	FNIP2 (I425M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517322	NM_020840.3(FNIP2):c.1319C>T (p.Ala440Val)	FNIP2 (A440V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476912	NM_020840.3(FNIP2):c.1351A>G (p.Thr451Ala)	FNIP2 (T97A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096135	NM_020840.3(FNIP2):c.1402A>G (p.Thr468Ala)	FNIP2 (T114A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 708521	NM_020840.3(FNIP2):c.1476C>T (p.Tyr492=)	FNIP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3096136	NM_020840.3(FNIP2):c.1519G>A (p.Val507Ile)	FNIP2 (V530I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223991	NM_020840.3(FNIP2):c.1531A>G (p.Lys511Glu)	FNIP2 (K157E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279440	NM_020840.3(FNIP2):c.1573C>T (p.Leu525Phe)	FNIP2 (L171F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 774858	NM_020840.3(FNIP2):c.1615G>C (p.Gly539Arg)	FNIP2 (G562R +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2528101	NM_020840.3(FNIP2):c.1625G>A (p.Gly542Asp)	FNIP2 (G188D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400980	NM_020840.3(FNIP2):c.1625G>C (p.Gly542Ala)	FNIP2 (G542A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096137	NM_020840.3(FNIP2):c.1712C>T (p.Thr571Met)	FNIP2 (T571M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655159	NM_020840.3(FNIP2):c.1713G>A (p.Thr571=)	FNIP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3096138	NM_020840.3(FNIP2):c.1732C>G (p.Leu578Val)	FNIP2 (L601V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271196	NM_020840.3(FNIP2):c.1754C>A (p.Pro585Gln)	FNIP2 (P638Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591048	NM_020840.3(FNIP2):c.1822A>G (p.Arg608Gly)	FNIP2 (R254G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511628	NM_020840.3(FNIP2):c.1891G>A (p.Ala631Thr)	FNIP2 (A631T +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 715499	NM_020840.3(FNIP2):c.1893A>G (p.Ala631=)	FNIP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3096139	NM_020840.3(FNIP2):c.1898G>T (p.Cys633Phe)	FNIP2 (C279F +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3096140	NM_020840.3(FNIP2):c.1918G>A (p.Ala640Thr)	FNIP2 (A693T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609019	NM_020840.3(FNIP2):c.1970C>G (p.Ala657Gly)	FNIP2 (A680G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096141	NM_020840.3(FNIP2):c.2014G>A (p.Gly672Arg)	FNIP2 (G318R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096142	NM_020840.3(FNIP2):c.2039A>G (p.Gln680Arg)	FNIP2 (Q703R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362086	NM_020840.3(FNIP2):c.2062G>A (p.Val688Met)	FNIP2 (V334M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314299	NM_020840.3(FNIP2):c.2070G>A (p.Met690Ile)	FNIP2 (M336I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520682	NM_020840.3(FNIP2):c.2089C>T (p.Arg697Trp)	FNIP2 (R720W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279441	NM_020840.3(FNIP2):c.2123T>C (p.Leu708Pro)	FNIP2 (L761P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096143	NM_020840.3(FNIP2):c.2125C>T (p.Arg709Trp)	FNIP2 (R732W +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2209926	NM_020840.3(FNIP2):c.2126G>A (p.Arg709Gln)	FNIP2 (R355Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510932	NM_020840.3(FNIP2):c.2201G>A (p.Arg734His)	FNIP2 (R380H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490775	NM_020840.3(FNIP2):c.2213T>C (p.Met738Thr)	FNIP2 (M384T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096144	NM_020840.3(FNIP2):c.2220A>T (p.Glu740Asp)	FNIP2 (E386D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 774444	NM_020840.3(FNIP2):c.2222G>A (p.Arg741Gln)	FNIP2 (R387Q +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2262847	NM_020840.3(FNIP2):c.2324A>G (p.Asn775Ser)	FNIP2 (N828S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096145	NM_020840.3(FNIP2):c.2344C>T (p.Arg782Trp)	FNIP2 (R805W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279444	NM_020840.3(FNIP2):c.2354A>G (p.Glu785Gly)	FNIP2 (E785G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096146	NM_020840.3(FNIP2):c.2368G>A (p.Glu790Lys)	FNIP2 (E436K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270712	NM_020840.3(FNIP2):c.2371T>A (p.Ser791Thr)	FNIP2 (S814T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528970	NM_020840.3(FNIP2):c.2413A>G (p.Met805Val)	FNIP2 (M805V +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2329588	NM_020840.3(FNIP2):c.2449G>A (p.Ala817Thr)	FNIP2 (A840T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096147	NM_020840.3(FNIP2):c.2465C>T (p.Ala822Val)	FNIP2 (A468V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308903	NM_020840.3(FNIP2):c.2540G>A (p.Gly847Glu)	FNIP2 (G493E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096149	NM_020840.3(FNIP2):c.2584C>T (p.Pro862Ser)	FNIP2 (P915S +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3096150	NM_020840.3(FNIP2):c.2593G>A (p.Val865Met)	FNIP2 (V511M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316739	NM_020840.3(FNIP2):c.2630A>G (p.Lys877Arg)	FNIP2 (K900R +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2461361	NM_020840.3(FNIP2):c.2768T>C (p.Leu923Ser)	FNIP2 (L946S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492743	NM_020840.3(FNIP2):c.2833C>T (p.Arg945Cys)	FNIP2 (R591C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279445	NM_020840.3(FNIP2):c.2927C>T (p.Ala976Val)	FNIP2 (A1029V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368090	NM_020840.3(FNIP2):c.3010T>C (p.Trp1004Arg)	FNIP2 (W650R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279443	NM_020840.3(FNIP2):c.3014G>T (p.Ser1005Ile)	FNIP2 (S1005I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279495	NM_020840.3(FNIP2):c.3047C>T (p.Thr1016Met)	FNIP2 (T1039M +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2520592	NM_020840.3(FNIP2):c.3055A>G (p.Met1019Val)	FNIP2 (M1042V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618632	NM_020840.3(FNIP2):c.3097A>G (p.Ser1033Gly)	FNIP2 (S1056G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348177	NM_020840.3(FNIP2):c.3112A>G (p.Ile1038Val)	FNIP2 (I1038V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 69