"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "FNIP1"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2794304	NM_133372.3(FNIP1):c.3423-8T>C	FNIP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2964775	NM_133372.3(FNIP1):c.3423-15T>C	FNIP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2413988	NM_133372.3(FNIP1):c.3422+15T>C	FNIP1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1950068	NM_133372.3(FNIP1):c.3389G>A (p.Arg1130His)	FNIP1 (R1102H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2111800	NM_133372.3(FNIP1):c.3381G>A (p.Gly1127=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1991141	NM_133372.3(FNIP1):c.3381G>T (p.Gly1127=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2082517	NM_133372.3(FNIP1):c.3317A>G (p.His1106Arg)	FNIP1 (H1106R +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2819351	NM_133372.3(FNIP1):c.3307-14C>T	FNIP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1928231	NM_133372.3(FNIP1):c.3306+17C>T	FNIP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2082760	NM_133372.3(FNIP1):c.3306+8T>C	FNIP1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2070880	NM_133372.3(FNIP1):c.3298C>T (p.Pro1100Ser)	FNIP1 (P1055S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2004500	NM_133372.3(FNIP1):c.3289A>G (p.Asn1097Asp)	FNIP1 (N1069D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1983061	NM_133372.3(FNIP1):c.3242G>T (p.Ser1081Ile)	FNIP1 (S1053I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3012554	NM_133372.3(FNIP1):c.3232T>C (p.Leu1078=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2071024	NM_133372.3(FNIP1):c.3200G>A (p.Arg1067Gln)	FNIP1 (R1022Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2062808	NM_133372.3(FNIP1):c.3152T>C (p.Ile1051Thr)	FNIP1 (I1006T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2194285	NM_133372.3(FNIP1):c.3135A>G (p.Ala1045=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1908559	NM_133372.3(FNIP1):c.3109-5T>C	FNIP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2797002	NM_133372.3(FNIP1):c.3108+19T>C	FNIP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2184338	NM_133372.3(FNIP1):c.3093A>G (p.Leu1031=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2168961	NM_133372.3(FNIP1):c.3088G>C (p.Asp1030His)	FNIP1 (D985H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2717996	NM_133372.3(FNIP1):c.3051T>C (p.Ile1017=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2038518	NM_133372.3(FNIP1):c.3024T>C (p.Tyr1008=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1943241	NM_133372.3(FNIP1):c.3015C>T (p.Cys1005=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2042809	NM_133372.3(FNIP1):c.2991G>A (p.Gly997=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1985860	NM_133372.3(FNIP1):c.2988C>T (p.Phe996=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2001192	NM_133372.3(FNIP1):c.2973C>T (p.Pro991=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2043596	NM_133372.3(FNIP1):c.2940-6_2940-4del	FNIP1	Microsatellite (intron variant)	not provided	GBenign
Select item 2814052	NM_133372.3(FNIP1):c.2940-15G>A	FNIP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2030667	NM_133372.3(FNIP1):c.2940-16G>A	FNIP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2788957	NM_133372.3(FNIP1):c.2940-20del	FNIP1	Deletion (intron variant)	not provided	GBenign
Select item 2025700	NM_133372.3(FNIP1):c.2922dup (p.Glu975Ter)	FNIP1 (E930* +2 more)	Duplication (nonsense)	not provided	GPathogenic
Select item 2042168	NM_133372.3(FNIP1):c.2911G>T (p.Ala971Ser)	FNIP1 (A943S +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2010810	NM_133372.3(FNIP1):c.2899C>A (p.Gln967Lys)	FNIP1 (Q967K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2085521	NM_133372.3(FNIP1):c.2869A>G (p.Arg957Gly)	FNIP1 (R912G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1983998	NM_133372.3(FNIP1):c.2855G>T (p.Gly952Val)	FNIP1 (G924V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2065453	NM_133372.3(FNIP1):c.2850T>C (p.Asp950=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2031591	NM_133372.3(FNIP1):c.2833dup (p.Asp945fs)	FNIP1 (D917fs +2 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 1925492	NM_133372.3(FNIP1):c.2797A>C (p.Ile933Leu)	FNIP1 (I888L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2802760	NM_133372.3(FNIP1):c.2790A>G (p.Glu930=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2063826	NM_133372.3(FNIP1):c.2786C>G (p.Thr929Ser)	FNIP1 (T929S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2043718	NM_133372.3(FNIP1):c.2779G>A (p.Val927Ile)	FNIP1 (V927I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2065554	NM_133372.3(FNIP1):c.2739C>A (p.Val913=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2842015	NM_133372.3(FNIP1):c.2724A>G (p.Thr908=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2034954	NM_133372.3(FNIP1):c.2721T>C (p.Asp907=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2042018	NM_133372.3(FNIP1):c.2712C>G (p.Asp904Glu)	FNIP1 (D859E +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2079395	NM_133372.3(FNIP1):c.2697C>T (p.Cys899=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2104130	NM_133372.3(FNIP1):c.2668A>G (p.Thr890Ala)	FNIP1 (T862A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2045748	NM_133372.3(FNIP1):c.2650T>C (p.Phe884Leu)	FNIP1 (F856L +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2776786	NM_133372.3(FNIP1):c.2649A>T (p.Glu883Asp)	FNIP1 (E855D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1968742	NM_133372.3(FNIP1):c.2646T>C (p.Asn882=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2101001	NM_133372.3(FNIP1):c.2630A>G (p.Asn877Ser)	FNIP1 (N877S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2803920	NM_133372.3(FNIP1):c.2597T>C (p.Met866Thr)	FNIP1 (M821T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2910673	NM_133372.3(FNIP1):c.2584G>A (p.Asp862Asn)	FNIP1 (D834N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2769963	NM_133372.3(FNIP1):c.2583A>G (p.Lys861=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3006764	NM_133372.3(FNIP1):c.2544T>G (p.Thr848=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2200499	NM_133372.3(FNIP1):c.2533G>A (p.Glu845Lys)	FNIP1 (E800K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2082849	NM_133372.3(FNIP1):c.2532C>T (p.Ile844=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1909615	NM_133372.3(FNIP1):c.2532C>A (p.Ile844=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2049173	NM_133372.3(FNIP1):c.2530A>G (p.Ile844Val)	FNIP1 (I799V +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2889069	NM_133372.3(FNIP1):c.2520T>C (p.Asn840=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1927832	NM_133372.3(FNIP1):c.2508C>T (p.Asp836=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2995743	NM_133372.3(FNIP1):c.2505C>T (p.Phe835=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2116300	NM_133372.3(FNIP1):c.2465C>T (p.Pro822Leu)	FNIP1 (P777L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1903402	NM_133372.3(FNIP1):c.2436C>T (p.Asn812=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2038942	NM_133372.3(FNIP1):c.2427T>C (p.Asp809=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2047649	NM_133372.3(FNIP1):c.2412A>G (p.Gln804=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2991523	NM_133372.3(FNIP1):c.2403C>G (p.Thr801=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1901818	NM_133372.3(FNIP1):c.2390C>T (p.Thr797Ile)	FNIP1 (T797I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2748584	NM_133372.3(FNIP1):c.2385A>G (p.Gln795=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2194613	NM_133372.3(FNIP1):c.2372T>C (p.Ile791Thr)	FNIP1 (I791T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2971049	NM_133372.3(FNIP1):c.2367G>A (p.Gly789=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2184098	NM_133372.3(FNIP1):c.2366G>A (p.Gly789Glu)	FNIP1 (G789E +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1940477	NM_133372.3(FNIP1):c.2356G>A (p.Glu786Lys)	FNIP1 (E741K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2040599	NM_133372.3(FNIP1):c.2350T>C (p.Leu784=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2120017	NM_133372.3(FNIP1):c.2325G>C (p.Gln775His)	FNIP1 (Q775H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1906807	NM_133372.3(FNIP1):c.2282C>T (p.Pro761Leu)	FNIP1 (P733L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1920062	NM_133372.3(FNIP1):c.2274T>C (p.Ser758=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977807	NM_133372.3(FNIP1):c.2235G>A (p.Glu745=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2038943	NM_133372.3(FNIP1):c.2212G>T (p.Val738Leu)	FNIP1 (V710L +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2109869	NM_133372.3(FNIP1):c.2191A>C (p.Lys731Gln)	FNIP1 (K686Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1906270	NM_133372.3(FNIP1):c.2189A>G (p.Glu730Gly)	FNIP1 (E702G +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2957659	NM_133372.3(FNIP1):c.2178A>G (p.Gly726=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2055518	NM_133372.3(FNIP1):c.2174C>T (p.Thr725Ile)	FNIP1 (T725I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2722530	NM_133372.3(FNIP1):c.2115A>C (p.Thr705=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2804561	NM_133372.3(FNIP1):c.2108_2109del (p.Glu703fs)	FNIP1 (E658fs +2 more)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 2093035	NM_133372.3(FNIP1):c.2105C>G (p.Thr702Arg)	FNIP1 (T657R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1946582	NM_133372.3(FNIP1):c.2105C>T (p.Thr702Ile)	FNIP1 (T702I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2057959	NM_133372.3(FNIP1):c.2099A>G (p.Glu700Gly)	FNIP1 (E655G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2045597	NM_133372.3(FNIP1):c.2098G>C (p.Glu700Gln)	FNIP1 (E700Q +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2189031	NM_133372.3(FNIP1):c.2064A>G (p.Pro688=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1936931	NM_133372.3(FNIP1):c.2051C>T (p.Thr684Ile)	FNIP1 (T656I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1950866	NM_133372.3(FNIP1):c.2044G>T (p.Val682Phe)	FNIP1 (V654F +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2046503	NM_133372.3(FNIP1):c.2025C>T (p.Asp675=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2067623	NM_133372.3(FNIP1):c.2005A>G (p.Lys669Glu)	FNIP1 (K641E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2079019	NM_133372.3(FNIP1):c.2000G>C (p.Arg667Thr)	FNIP1 (R639T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2195235	NM_133372.3(FNIP1):c.1997A>G (p.Tyr666Cys)	FNIP1 (Y621C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1929992	NM_133372.3(FNIP1):c.1981G>A (p.Val661Ile)	FNIP1 (V616I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2023852	NM_133372.3(FNIP1):c.1960G>A (p.Asp654Asn)	FNIP1 (D626N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3022172	NM_133372.3(FNIP1):c.1953T>C (p.Ser651=)	FNIP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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