Related gene-specific medical variations for Gene (Select 107985781) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 287

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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, FSIP2-AS1 (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 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 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 3097274	NM_173651.4(FSIP2):c.2302T>C (p.Ser768Pro)	FSIP2, FSIP2-AS1 (S768P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097273	NM_173651.4(FSIP2):c.2269G>A (p.Glu757Lys)	FSIP2, FSIP2-AS1 (E757K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097272	NM_173651.4(FSIP2):c.2174C>G (p.Ser725Cys)	FSIP2, FSIP2-AS1 (S725C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097270	NM_173651.4(FSIP2):c.1948T>G (p.Leu650Val)	FSIP2, FSIP2-AS1 (L650V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097267	NM_173651.4(FSIP2):c.1792C>T (p.Pro598Ser)	FSIP2, FSIP2-AS1 (P598S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097263	NM_173651.4(FSIP2):c.1711T>C (p.Tyr571His)	FSIP2, FSIP2-AS1 (Y571H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097210	NM_173651.4(FSIP2):c.10715A>T (p.Lys3572Ile)	FSIP2, FSIP2-AS1 (K3572I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097209	NM_173651.4(FSIP2):c.10637T>A (p.Phe3546Tyr)	FSIP2, FSIP2-AS1 (F3546Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097208	NM_173651.4(FSIP2):c.10621A>G (p.Ile3541Val)	FSIP2, FSIP2-AS1 (I3541V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097206	NM_173651.4(FSIP2):c.10232A>G (p.Gln3411Arg)	FSIP2, FSIP2-AS1 (Q3411R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097205	NM_173651.4(FSIP2):c.10142T>G (p.Leu3381Trp)	FSIP2, FSIP2-AS1 (L3381W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097204	NM_173651.4(FSIP2):c.9979T>C (p.Cys3327Arg)	FSIP2, FSIP2-AS1 (C3327R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097202	NM_173651.4(FSIP2):c.9773T>C (p.Met3258Thr)	FSIP2, FSIP2-AS1 (M3258T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3065719	NM_173651.4(FSIP2):c.2680_2693del (p.Asn894fs)	FSIP2, FSIP2-AS1 (N894fs)	Deletion (frameshift variant)	Spermatogenic failure 34	GLikely pathogenic
Select item 3060908	NM_173651.4(FSIP2):c.2729A>G (p.Asn910Ser)	FSIP2, FSIP2-AS1 (N910S)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3060901	NM_173651.4(FSIP2):c.5093T>C (p.Met1698Thr)	FSIP2, FSIP2-AS1 (M1698T)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3060809	NM_173651.4(FSIP2):c.9810A>G (p.Leu3270=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GBenign
Select item 3060798	NM_173651.4(FSIP2):c.2455A>T (p.Ile819Phe)	FSIP2, FSIP2-AS1 (I819F)	Single nucleotide variant (missense variant)	FSIP2-related condition	GLikely benign
Select item 3060483	NM_173651.4(FSIP2):c.7321C>A (p.Gln2441Lys)	FSIP2, FSIP2-AS1 (Q2441K)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3060358	NM_173651.4(FSIP2):c.6575C>T (p.Thr2192Met)	FSIP2, FSIP2-AS1 (T2192M)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3060248	NM_173651.4(FSIP2):c.7496G>T (p.Arg2499Met)	FSIP2, FSIP2-AS1 (R2499M)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3060053	NM_173651.4(FSIP2):c.6702G>T (p.Glu2234Asp)	FSIP2, FSIP2-AS1 (E2234D)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3059914	NM_173651.4(FSIP2):c.4794C>T (p.Asn1598=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GBenign
Select item 3059835	NM_173651.4(FSIP2):c.5226C>A (p.Ser1742=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GBenign
Select item 3059707	NM_173651.4(FSIP2):c.6193G>A (p.Asp2065Asn)	FSIP2, FSIP2-AS1 (D2065N)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3059504	NM_173651.4(FSIP2):c.3863G>A (p.Arg1288Gln)	FSIP2, FSIP2-AS1 (R1288Q)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3059151	NM_173651.4(FSIP2):c.3004G>C (p.Asp1002His)	FSIP2, FSIP2-AS1 (D1002H)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
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 condition	GBenign
Select item 3058958	NM_173651.4(FSIP2):c.10440T>C (p.Tyr3480=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GBenign
Select item 3058814	NM_173651.4(FSIP2):c.8985G>T (p.Thr2995=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GLikely benign
Select item 3058661	NM_173651.4(FSIP2):c.2712T>C (p.Tyr904=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GLikely benign
Select item 3058393	NM_173651.4(FSIP2):c.10053G>A (p.Glu3351=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GLikely benign
Select item 3057160	NM_173651.4(FSIP2):c.4037C>T (p.Thr1346Met)	FSIP2, FSIP2-AS1 (T1346M)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3057096	NM_173651.4(FSIP2):c.7366T>C (p.Leu2456=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GLikely benign
Select item 3056953	NM_173651.4(FSIP2):c.8698A>G (p.Lys2900Glu)	FSIP2, FSIP2-AS1 (K2900E)	Single nucleotide variant (missense variant)	FSIP2-related condition	GLikely benign
Select item 3056841	NM_173651.4(FSIP2):c.5522T>C (p.Ile1841Thr)	FSIP2, FSIP2-AS1 (I1841T)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3056805	NM_173651.4(FSIP2):c.4977T>C (p.Asn1659=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GBenign
Select item 3055933	NM_173651.4(FSIP2):c.10233A>G (p.Gln3411=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GBenign
Select item 3055842	NM_173651.4(FSIP2):c.6923A>T (p.Asp2308Val)	FSIP2, FSIP2-AS1 (D2308V)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3055639	NM_173651.4(FSIP2):c.5026A>T (p.Thr1676Ser)	FSIP2, FSIP2-AS1 (T1676S)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3055485	NM_173651.4(FSIP2):c.8878T>C (p.Phe2960Leu)	FSIP2, FSIP2-AS1 (F2960L)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3055383	NM_173651.4(FSIP2):c.9704G>A (p.Cys3235Tyr)	FSIP2, FSIP2-AS1 (C3235Y)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3050999	NM_173651.4(FSIP2):c.8909C>T (p.Pro2970Leu)	FSIP2, FSIP2-AS1 (P2970L)	Single nucleotide variant (missense variant)	FSIP2-related condition	GLikely benign
Select item 3050785	NM_173651.4(FSIP2):c.5367T>C (p.Phe1789=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GBenign
Select item 3049697	NM_173651.4(FSIP2):c.6194A>G (p.Asp2065Gly)	FSIP2, FSIP2-AS1 (D2065G)	Single nucleotide variant (missense variant)	FSIP2-related condition	GLikely benign
Select item 3045872	NM_173651.4(FSIP2):c.9733A>C (p.Arg3245=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GLikely benign
Select item 3044487	NM_173651.4(FSIP2):c.10014A>C (p.Leu3338=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GLikely benign
Select item 3043394	NM_173651.4(FSIP2):c.8958C>T (p.Asn2986=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	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 condition	GBenign
Select item 3041888	NM_173651.4(FSIP2):c.3794G>A (p.Arg1265His)	FSIP2, FSIP2-AS1 (R1265H)	Single nucleotide variant (missense variant)	FSIP2-related condition	GBenign
Select item 3039454	NM_173651.4(FSIP2):c.3642A>C (p.Ala1214=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GLikely benign
Select item 3039066	NM_173651.4(FSIP2):c.10212G>A (p.Arg3404=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GLikely benign
Select item 3038725	NM_173651.4(FSIP2):c.10710T>C (p.Asn3570=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	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 condition	GBenign
Select item 3037644	NM_173651.4(FSIP2):c.8046A>G (p.Leu2682=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	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 condition	GLikely benign
Select item 3034979	NM_173651.4(FSIP2):c.2091A>G (p.Lys697=)	FSIP2-AS1, FSIP2	Single nucleotide variant (synonymous variant)	FSIP2-related condition	GBenign
Select item 3034750	NM_173651.4(FSIP2):c.7539C>T (p.Asn2513=)	FSIP2, FSIP2-AS1	Single nucleotide variant (synonymous variant)	FSIP2-related condition	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 condition	GBenign
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 condition	GBenign

<< First< Prev

Page of 3