ClinVar for Gene (Select 401024) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3383076	NM_173651.4(FSIP2):c.6060del (p.Glu2021fs)	FSIP2, FSIP2-AS1 (E2021fs)	Deletion (frameshift variant)	Spermatogenic failure 34	GPathogenic
Select item 3383075	NM_173651.4(FSIP2):c.11998G>A (p.Val4000Met)	FSIP2 (V4000M)	Single nucleotide variant (missense variant)	Spermatogenic failure 34	GUncertain significance
Select item 3356032	NM_173651.4(FSIP2):c.8003C>A (p.Ser2668Ter)	FSIP2, FSIP2-AS1 (S2668*)	Single nucleotide variant (nonsense)	FSIP2-related disorder	GPathogenic
Select item 3352490	NM_173651.4(FSIP2):c.9363C>T (p.Ile3121=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related disorder	GLikely benign
Select item 3352098	NM_173651.4(FSIP2):c.15982del (p.Ile5328fs)	FSIP2 (I5328fs)	Deletion (frameshift variant)	FSIP2-related disorder	GLikely pathogenic
Select item 3348464	NM_173651.4(FSIP2):c.11999T>G (p.Val4000Gly)	FSIP2 (V4000G)	Single nucleotide variant (missense variant)	FSIP2-related disorder	GUncertain significance
Select item 3280097	NM_173651.4(FSIP2):c.4540G>C (p.Glu1514Gln)	FSIP2, FSIP2-AS1 (E1514Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280096	NM_173651.4(FSIP2):c.9961A>G (p.Ile3321Val)	FSIP2, FSIP2-AS1 (I3321V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3280095	NM_173651.4(FSIP2):c.193G>A (p.Ala65Thr)	FSIP2, FSIP2-AS2 (A65T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3280094	NM_173651.4(FSIP2):c.19359A>C (p.Lys6453Asn)	FSIP2 (K6453N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280093	NM_173651.4(FSIP2):c.14626A>G (p.Ile4876Val)	FSIP2 (I4876V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280092	NM_173651.4(FSIP2):c.8749G>C (p.Gly2917Arg)	FSIP2, FSIP2-AS1 (G2917R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280091	NM_173651.4(FSIP2):c.9216T>A (p.His3072Gln)	FSIP2, FSIP2-AS1 (H3072Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280090	NM_173651.4(FSIP2):c.15559A>G (p.Ile5187Val)	FSIP2 (I5187V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280089	NM_173651.4(FSIP2):c.8965G>T (p.Val2989Phe)	FSIP2, FSIP2-AS1 (V2989F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280087	NM_173651.4(FSIP2):c.12338T>C (p.Ile4113Thr)	FSIP2 (I4113T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280086	NM_173651.4(FSIP2):c.18349A>C (p.Ile6117Leu)	FSIP2 (I6117L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280085	NM_173651.4(FSIP2):c.9298G>C (p.Glu3100Gln)	FSIP2, FSIP2-AS1 (E3100Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280084	NM_173651.4(FSIP2):c.6470A>G (p.Asn2157Ser)	FSIP2, FSIP2-AS1 (N2157S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280083	NM_173651.4(FSIP2):c.10553C>T (p.Thr3518Ile)	FSIP2, FSIP2-AS1 (T3518I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280082	NM_173651.4(FSIP2):c.9535A>G (p.Asn3179Asp)	FSIP2, FSIP2-AS1 (N3179D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280081	NM_173651.4(FSIP2):c.13538T>A (p.Ile4513Asn)	FSIP2 (I4513N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280080	NM_173651.4(FSIP2):c.10573G>A (p.Glu3525Lys)	FSIP2, FSIP2-AS1 (E3525K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280079	NM_173651.4(FSIP2):c.10777C>A (p.Pro3593Thr)	FSIP2, FSIP2-AS1 (P3593T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3280078	NM_173651.4(FSIP2):c.8183C>G (p.Thr2728Arg)	FSIP2, FSIP2-AS1 (T2728R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280076	NM_173651.4(FSIP2):c.7601A>G (p.His2534Arg)	FSIP2, FSIP2-AS1 (H2534R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280075	NM_173651.4(FSIP2):c.16360G>A (p.Asp5454Asn)	FSIP2 (D5454N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280074	NM_173651.4(FSIP2):c.7934C>T (p.Ser2645Leu)	FSIP2, FSIP2-AS1 (S2645L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280073	NM_173651.4(FSIP2):c.16355C>A (p.Thr5452Asn)	FSIP2 (T5452N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280072	NM_173651.4(FSIP2):c.17656T>C (p.Ser5886Pro)	FSIP2 (S5886P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280071	NM_173651.4(FSIP2):c.2545A>C (p.Asn849His)	FSIP2, FSIP2-AS1 (N849H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280070	NM_173651.4(FSIP2):c.17401T>C (p.Ser5801Pro)	FSIP2 (S5801P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280069	NM_173651.4(FSIP2):c.16556A>G (p.Glu5519Gly)	FSIP2 (E5519G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280068	NM_173651.4(FSIP2):c.19465G>C (p.Val6489Leu)	FSIP2 (V6489L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280067	NM_173651.4(FSIP2):c.10180G>A (p.Glu3394Lys)	FSIP2, FSIP2-AS1 (E3394K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280065	NM_173651.4(FSIP2):c.3351G>A (p.Met1117Ile)	FSIP2, FSIP2-AS1 (M1117I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280064	NM_173651.4(FSIP2):c.15220G>C (p.Val5074Leu)	FSIP2 (V5074L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280063	NM_173651.4(FSIP2):c.6151C>T (p.Arg2051Cys)	FSIP2, FSIP2-AS1 (R2051C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3280062	NM_173651.4(FSIP2):c.1418A>T (p.Gln473Leu)	FSIP2 (Q473L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280061	NM_173651.4(FSIP2):c.14077G>A (p.Val4693Ile)	FSIP2 (V4693I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280060	NM_173651.4(FSIP2):c.10408A>T (p.Met3470Leu)	FSIP2, FSIP2-AS1 (M3470L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280059	NM_173651.4(FSIP2):c.11639T>C (p.Ile3880Thr)	FSIP2 (I3880T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280058	NM_173651.4(FSIP2):c.1967G>T (p.Gly656Val)	FSIP2, FSIP2-AS1 (G656V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280056	NM_173651.4(FSIP2):c.9835G>A (p.Asp3279Asn)	FSIP2, FSIP2-AS1 (D3279N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280055	NM_173651.4(FSIP2):c.14165A>G (p.Asp4722Gly)	FSIP2 (D4722G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280054	NM_173651.4(FSIP2):c.2999A>T (p.Tyr1000Phe)	FSIP2, FSIP2-AS1 (Y1000F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280053	NM_173651.4(FSIP2):c.10780G>A (p.Gly3594Arg)	FSIP2, FSIP2-AS1 (G3594R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3280052	NM_173651.4(FSIP2):c.15632A>T (p.Asp5211Val)	FSIP2 (D5211V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280051	NM_173651.4(FSIP2):c.658C>T (p.Arg220Cys)	FSIP2 (R220C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280050	NM_173651.4(FSIP2):c.16991C>T (p.Thr5664Met)	FSIP2 (T5664M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280049	NM_173651.4(FSIP2):c.16624A>G (p.Thr5542Ala)	FSIP2 (T5542A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3239649	NM_173651.4(FSIP2):c.2689del (p.Ser897fs)	FSIP2, FSIP2-AS1 (S897fs)	Deletion (frameshift variant)	Abnormal sperm morphology +2 more	GPathogenic
Select item 3097326	NM_173651.4(FSIP2):c.9605T>C (p.Val3202Ala)	FSIP2, FSIP2-AS1 (V3202A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097325	NM_173651.4(FSIP2):c.713G>A (p.Arg238Gln)	FSIP2 (R238Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097324	NM_173651.4(FSIP2):c.9533T>C (p.Ile3178Thr)	FSIP2, FSIP2-AS1 (I3178T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097323	NM_173651.4(FSIP2):c.9418C>G (p.Leu3140Val)	FSIP2, FSIP2-AS1 (L3140V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097322	NM_173651.4(FSIP2):c.8613A>G (p.Ile2871Met)	FSIP2, FSIP2-AS1 (I2871M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097321	NM_173651.4(FSIP2):c.8446G>A (p.Ala2816Thr)	FSIP2, FSIP2-AS1 (A2816T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097319	NM_173651.4(FSIP2):c.602G>A (p.Arg201Gln)	FSIP2 (R201Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097318	NM_173651.4(FSIP2):c.8431C>A (p.Leu2811Ile)	FSIP2, FSIP2-AS1 (L2811I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097317	NM_173651.4(FSIP2):c.8417T>C (p.Ile2806Thr)	FSIP2, FSIP2-AS1 (I2806T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097316	NM_173651.4(FSIP2):c.8387C>T (p.Ser2796Phe)	FSIP2, FSIP2-AS1 (S2796F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3097315	NM_173651.4(FSIP2):c.586A>G (p.Ile196Val)	FSIP2 (I196V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097314	NM_173651.4(FSIP2):c.8164G>A (p.Ala2722Thr)	FSIP2, FSIP2-AS1 (A2722T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097313	NM_173651.4(FSIP2):c.7366T>A (p.Leu2456Met)	FSIP2, FSIP2-AS1 (L2456M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097312	NM_173651.4(FSIP2):c.7010T>C (p.Leu2337Pro)	FSIP2, FSIP2-AS1 (L2337P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097310	NM_173651.4(FSIP2):c.6935T>A (p.Leu2312Gln)	FSIP2, FSIP2-AS1 (L2312Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097309	NM_173651.4(FSIP2):c.6836G>A (p.Ser2279Asn)	FSIP2, FSIP2-AS1 (S2279N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097308	NM_173651.4(FSIP2):c.6698T>C (p.Val2233Ala)	FSIP2, FSIP2-AS1 (V2233A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097307	NM_173651.4(FSIP2):c.6535A>C (p.Asn2179His)	FSIP2, FSIP2-AS1 (N2179H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097306	NM_173651.2(FSIP2):c.67C>T (p.Leu23Phe)	FSIP2, FSIP2-AS2 (L23F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097305	NM_173651.4(FSIP2):c.6308A>T (p.Glu2103Val)	FSIP2, FSIP2-AS1 (E2103V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097304	NM_173651.4(FSIP2):c.5954A>C (p.Lys1985Thr)	FSIP2, FSIP2-AS1 (K1985T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097303	NM_173651.4(FSIP2):c.5765A>G (p.Gln1922Arg)	FSIP2, FSIP2-AS1 (Q1922R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097302	NM_173651.4(FSIP2):c.5575A>G (p.Met1859Val)	FSIP2, FSIP2-AS1 (M1859V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097301	NM_173651.4(FSIP2):c.5504C>T (p.Ser1835Leu)	FSIP2, FSIP2-AS1 (S1835L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097300	NM_173651.4(FSIP2):c.5453C>T (p.Thr1818Ile)	FSIP2, FSIP2-AS1 (T1818I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3097299	NM_173651.4(FSIP2):c.5336C>T (p.Pro1779Leu)	FSIP2, FSIP2-AS1 (P1779L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097297	NM_173651.4(FSIP2):c.5223A>T (p.Arg1741Ser)	FSIP2, FSIP2-AS1 (R1741S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097296	NM_173651.4(FSIP2):c.5188G>T (p.Asp1730Tyr)	FSIP2, FSIP2-AS1 (D1730Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097295	NM_173651.4(FSIP2):c.4897G>A (p.Ala1633Thr)	FSIP2, FSIP2-AS1 (A1633T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097294	NM_173651.4(FSIP2):c.4846A>C (p.Lys1616Gln)	FSIP2, FSIP2-AS1 (K1616Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097293	NM_173651.4(FSIP2):c.4574C>T (p.Ser1525Leu)	FSIP2, FSIP2-AS1 (S1525L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097292	NM_173651.4(FSIP2):c.4534A>G (p.Ile1512Val)	FSIP2, FSIP2-AS1 (I1512V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3097291	NM_173651.4(FSIP2):c.4408C>A (p.Gln1470Lys)	FSIP2, FSIP2-AS1 (Q1470K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097290	NM_173651.4(FSIP2):c.4407T>A (p.Asn1469Lys)	FSIP2, FSIP2-AS1 (N1469K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097289	NM_173651.4(FSIP2):c.4267C>T (p.His1423Tyr)	FSIP2, FSIP2-AS1 (H1423Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097288	NM_173651.4(FSIP2):c.3932A>C (p.Glu1311Ala)	FSIP2-AS1, FSIP2 (E1311A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097286	NM_173651.4(FSIP2):c.3851A>G (p.Lys1284Arg)	FSIP2, FSIP2-AS1 (K1284R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097285	NM_173651.4(FSIP2):c.3793C>T (p.Arg1265Cys)	FSIP2, FSIP2-AS1 (R1265C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097283	NM_173651.4(FSIP2):c.3313G>C (p.Ala1105Pro)	FSIP2, FSIP2-AS1 (A1105P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097282	NM_173651.4(FSIP2):c.86A>G (p.Gln29Arg)	FSIP2, FSIP2-AS2 +1 more (Q29R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097281	NM_173651.4(FSIP2):c.3140G>T (p.Arg1047Ile)	FSIP2, FSIP2-AS1 (R1047I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097280	NM_173651.4(FSIP2):c.3109A>G (p.Thr1037Ala)	FSIP2, FSIP2-AS1 (T1037A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097279	NM_173651.2(FSIP2):c.31A>G (p.Arg11Gly)	FSIP2, FSIP2-AS2 (R11G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097278	NM_173651.4(FSIP2):c.2813T>C (p.Leu938Pro)	FSIP2, FSIP2-AS1 (L938P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097277	NM_173651.4(FSIP2):c.2632G>C (p.Asp878His)	FSIP2, FSIP2-AS1 (D878H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097276	NM_173651.4(FSIP2):c.2454T>A (p.Asp818Glu)	FSIP2, FSIP2-AS1 (D818E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097275	NM_173651.4(FSIP2):c.-11C>T	FSIP2, FSIP2-AS2	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3097274	NM_173651.4(FSIP2):c.2302T>C (p.Ser768Pro)	FSIP2, FSIP2-AS1 (S768P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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