"FSIP2-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039107	NM_173651.4(FSIP2):c.-4G>A	FSIP2, FSIP2-AS2	Single nucleotide variant (5 prime UTR variant)	FSIP2-related disorder	GLikely benign
Select item 3057992	NM_173651.4(FSIP2):c.99C>T (p.Asp33=)	FSIP2, FSIP2-AS2 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	FSIP2-related disorder	GLikely benign
Select item 3050642	NM_173651.4(FSIP2):c.277T>C (p.Leu93=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3042041	NM_173651.4(FSIP2):c.417G>A (p.Lys139=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3056516	NM_173651.4(FSIP2):c.712C>T (p.Arg238Trp)	FSIP2 (R238W)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3033838	NM_173651.4(FSIP2):c.717A>G (p.Glu239=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3039528	NM_173651.4(FSIP2):c.916A>G (p.Met306Val)	FSIP2 (M306V)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 3034749	NM_173651.4(FSIP2):c.1069G>C (p.Glu357Gln)	FSIP2 (E357Q)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3055476	NM_173651.4(FSIP2):c.1131G>A (p.Thr377=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3059608	NM_173651.4(FSIP2):c.1134A>G (p.Lys378=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3050324	NM_173651.4(FSIP2):c.1195-8C>T	FSIP2	Single nucleotide variant (intron variant)	FSIP2-related disorder	GLikely benign
Select item 3049892	NM_173651.4(FSIP2):c.1217A>C (p.Asn406Thr)	FSIP2 (N406T)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 3034829	NM_173651.4(FSIP2):c.1217A>T (p.Asn406Ile)	FSIP2 (N406I)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 3059353	NM_173651.4(FSIP2):c.1274T>C (p.Ile425Thr)	FSIP2 (I425T)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3052408	NM_173651.4(FSIP2):c.1348-8T>C	FSIP2	Single nucleotide variant (intron variant)	FSIP2-related disorder	GLikely benign
Select item 3039858	NM_173651.4(FSIP2):c.1374A>G (p.Gly458=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3047623	NM_173651.4(FSIP2):c.1437G>A (p.Pro479=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3037631	NM_173651.4(FSIP2):c.1639G>A (p.Asp547Asn)	FSIP2, FSIP2-AS1 (D547N)	Single nucleotide variant (non-coding transcript variant +1 more)	FSIP2-related disorder	GLikely benign
Select item 1709917	NM_173651.4(FSIP2):c.1660_1662dup (p.Asp554_Ser555insAsp)	FSIP2, FSIP2-AS1	Duplication (non-coding transcript variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 3059073	NM_173651.4(FSIP2):c.1683G>A (p.Thr561=)	FSIP2, FSIP2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	FSIP2-related disorder	GBenign
Select item 1675831	NM_173651.4(FSIP2):c.1770G>A (p.Thr590=)	FSIP2, FSIP2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GLikely benign
Select item 3034979	NM_173651.4(FSIP2):c.2091A>G (p.Lys697=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 2590621	NM_173651.4(FSIP2):c.2219G>A (p.Arg740His)	FSIP2, FSIP2-AS1 (R740H)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3060798	NM_173651.4(FSIP2):c.2455A>T (p.Ile819Phe)	FSIP2, FSIP2-AS1 (I819F)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 3042458	NM_173651.4(FSIP2):c.2584T>C (p.Cys862Arg)	FSIP2, FSIP2-AS1 (C862R)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3058661	NM_173651.4(FSIP2):c.2712T>C (p.Tyr904=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3060908	NM_173651.4(FSIP2):c.2729A>G (p.Asn910Ser)	FSIP2, FSIP2-AS1 (N910S)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3059151	NM_173651.4(FSIP2):c.3004G>C (p.Asp1002His)	FSIP2, FSIP2-AS1 (D1002H)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3039454	NM_173651.4(FSIP2):c.3642A>C (p.Ala1214=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3041888	NM_173651.4(FSIP2):c.3794G>A (p.Arg1265His)	FSIP2, FSIP2-AS1 (R1265H)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3059504	NM_173651.4(FSIP2):c.3863G>A (p.Arg1288Gln)	FSIP2, FSIP2-AS1 (R1288Q)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3057160	NM_173651.4(FSIP2):c.4037C>T (p.Thr1346Met)	FSIP2, FSIP2-AS1 (T1346M)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3024948	NM_173651.4(FSIP2):c.4459A>G (p.Ile1487Val)	FSIP2, FSIP2-AS1 (I1487V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3059914	NM_173651.4(FSIP2):c.4794C>T (p.Asn1598=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3056805	NM_173651.4(FSIP2):c.4977T>C (p.Asn1659=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3055639	NM_173651.4(FSIP2):c.5026A>T (p.Thr1676Ser)	FSIP2, FSIP2-AS1 (T1676S)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3060901	NM_173651.4(FSIP2):c.5093T>C (p.Met1698Thr)	FSIP2, FSIP2-AS1 (M1698T)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3059835	NM_173651.4(FSIP2):c.5226C>A (p.Ser1742=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3050785	NM_173651.4(FSIP2):c.5367T>C (p.Phe1789=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3056841	NM_173651.4(FSIP2):c.5522T>C (p.Ile1841Thr)	FSIP2, FSIP2-AS1 (I1841T)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3059707	NM_173651.4(FSIP2):c.6193G>A (p.Asp2065Asn)	FSIP2, FSIP2-AS1 (D2065N)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3049697	NM_173651.4(FSIP2):c.6194A>G (p.Asp2065Gly)	FSIP2, FSIP2-AS1 (D2065G)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 1694999	NM_173651.4(FSIP2):c.6226C>A (p.Leu2076Met)	FSIP2, FSIP2-AS1 (L2076M)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3060358	NM_173651.4(FSIP2):c.6575C>T (p.Thr2192Met)	FSIP2, FSIP2-AS1 (T2192M)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3060053	NM_173651.4(FSIP2):c.6702G>T (p.Glu2234Asp)	FSIP2, FSIP2-AS1 (E2234D)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3055842	NM_173651.4(FSIP2):c.6923A>T (p.Asp2308Val)	FSIP2, FSIP2-AS1 (D2308V)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3060483	NM_173651.4(FSIP2):c.7321C>A (p.Gln2441Lys)	FSIP2, FSIP2-AS1 (Q2441K)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3057096	NM_173651.4(FSIP2):c.7366T>C (p.Leu2456=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3060248	NM_173651.4(FSIP2):c.7496G>T (p.Arg2499Met)	FSIP2, FSIP2-AS1 (R2499M)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3034750	NM_173651.4(FSIP2):c.7539C>T (p.Asn2513=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 1049600	NM_173651.4(FSIP2):c.7540T>C (p.Phe2514Leu)	FSIP2, FSIP2-AS1 (F2514L)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 2651746	NM_173651.4(FSIP2):c.7713T>C (p.Ser2571=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder +1 more	GLikely benign
Select item 3037644	NM_173651.4(FSIP2):c.8046A>G (p.Leu2682=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3034046	NM_173651.4(FSIP2):c.8149A>G (p.Met2717Val)	FSIP2, FSIP2-AS1 (M2717V)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3056953	NM_173651.4(FSIP2):c.8698A>G (p.Lys2900Glu)	FSIP2, FSIP2-AS1 (K2900E)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 3055485	NM_173651.4(FSIP2):c.8878T>C (p.Phe2960Leu)	FSIP2, FSIP2-AS1 (F2960L)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3050999	NM_173651.4(FSIP2):c.8909C>T (p.Pro2970Leu)	FSIP2, FSIP2-AS1 (P2970L)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 789270	NM_173651.4(FSIP2):c.8947G>A (p.Gly2983Ser)	FSIP2, FSIP2-AS1 (G2983S)	Single nucleotide variant (missense variant)	FSIP2-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3043394	NM_173651.4(FSIP2):c.8958C>T (p.Asn2986=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3058814	NM_173651.4(FSIP2):c.8985G>T (p.Thr2995=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3032624	NM_173651.4(FSIP2):c.9171T>C (p.Thr3057=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3037770	NM_173651.4(FSIP2):c.9313G>C (p.Glu3105Gln)	FSIP2, FSIP2-AS1 (E3105Q)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 1695000	NM_173651.4(FSIP2):c.9536A>G (p.Asn3179Ser)	FSIP2, FSIP2-AS1 (N3179S)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3055383	NM_173651.4(FSIP2):c.9704G>A (p.Cys3235Tyr)	FSIP2, FSIP2-AS1 (C3235Y)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3045872	NM_173651.4(FSIP2):c.9733A>C (p.Arg3245=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 1335430	NM_173651.4(FSIP2):c.9739A>G (p.Arg3247Gly)	FSIP2, FSIP2-AS1 (R3247G)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3060809	NM_173651.4(FSIP2):c.9810A>G (p.Leu3270=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3044487	NM_173651.4(FSIP2):c.10014A>C (p.Leu3338=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3058393	NM_173651.4(FSIP2):c.10053G>A (p.Glu3351=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3039066	NM_173651.4(FSIP2):c.10212G>A (p.Arg3404=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3055933	NM_173651.4(FSIP2):c.10233A>G (p.Gln3411=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3058958	NM_173651.4(FSIP2):c.10440T>C (p.Tyr3480=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 2582990	NM_173651.4(FSIP2):c.10470C>T (p.Tyr3490=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3038725	NM_173651.4(FSIP2):c.10710T>C (p.Asn3570=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3033924	NM_173651.4(FSIP2):c.10792G>A (p.Gly3598Ser)	FSIP2, FSIP2-AS1 (G3598S)	Single nucleotide variant (non-coding transcript variant +1 more)	FSIP2-related disorder	GBenign
Select item 3034005	NM_173651.4(FSIP2):c.10865A>G (p.Asp3622Gly)	FSIP2 (D3622G)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3059153	NM_173651.4(FSIP2):c.10930C>A (p.Leu3644Ile)	FSIP2 (L3644I)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3048367	NM_173651.4(FSIP2):c.11065A>G (p.Thr3689Ala)	FSIP2 (T3689A)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 2651748	NM_173651.4(FSIP2):c.11144C>T (p.Thr3715Met)	FSIP2 (T3715M)	Single nucleotide variant (missense variant)	FSIP2-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3055379	NM_173651.4(FSIP2):c.11158G>C (p.Gly3720Arg)	FSIP2 (G3720R)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3040372	NM_173651.4(FSIP2):c.11219C>A (p.Thr3740Asn)	FSIP2 (T3740N)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3060270	NM_173651.4(FSIP2):c.11399G>A (p.Gly3800Glu)	FSIP2 (G3800E)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3050763	NM_173651.4(FSIP2):c.11500T>C (p.Leu3834=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3040752	NM_173651.4(FSIP2):c.11745C>T (p.Ser3915=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3059854	NM_173651.4(FSIP2):c.11791A>G (p.Asn3931Asp)	FSIP2 (N3931D)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3039166	NM_173651.4(FSIP2):c.12310T>A (p.Ser4104Thr)	FSIP2 (S4104T)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 3055857	NM_173651.4(FSIP2):c.12381A>C (p.Leu4127=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3044465	NM_173651.4(FSIP2):c.12402T>C (p.Tyr4134=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3059670	NM_173651.4(FSIP2):c.13088T>C (p.Phe4363Ser)	FSIP2 (F4363S)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3059920	NM_173651.4(FSIP2):c.13327A>C (p.Ile4443Leu)	FSIP2 (I4443L)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3039766	NM_173651.4(FSIP2):c.13890T>G (p.Val4630=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GBenign
Select item 3059053	NM_173651.4(FSIP2):c.13920C>A (p.Gly4640=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3053724	NM_173651.4(FSIP2):c.13987C>T (p.His4663Tyr)	FSIP2 (H4663Y)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GLikely benign
Select item 3041868	NM_173651.4(FSIP2):c.14058A>G (p.Leu4686=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3055248	NM_173651.4(FSIP2):c.14188A>C (p.Ile4730Leu)	FSIP2 (I4730L)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3059502	NM_173651.4(FSIP2):c.14681A>T (p.Lys4894Ile)	FSIP2 (K4894I)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 2571112	NM_173651.4(FSIP2):c.14900A>T (p.Asn4967Ile)	FSIP2 (N4967I)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3039283	NM_173651.4(FSIP2):c.14901C>T (p.Asn4967=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3059379	NM_173651.4(FSIP2):c.14902A>G (p.Met4968Val)	FSIP2 (M4968V)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GBenign
Select item 3033782	NM_173651.4(FSIP2):c.15252G>A (p.Ser5084=)	FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign

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