ClinVar for Gene (Select 6405) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358635	NM_004186.5(SEMA3F):c.762C>T (p.Asn254=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3358624	NM_004186.5(SEMA3F):c.1764C>T (p.Asp588=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3358561	NM_004186.5(SEMA3F):c.2204C>A (p.Ala735Asp)	SEMA3F (A636D +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3358531	NM_004186.5(SEMA3F):c.2145G>A (p.Pro715=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3358417	NM_004186.5(SEMA3F):c.771G>A (p.Ser257=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3358386	NM_004186.5(SEMA3F):c.2348C>T (p.Pro783Leu)	SEMA3F (P684L +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3358378	NM_004186.5(SEMA3F):c.1047C>T (p.Asp349=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3358267	NM_004186.5(SEMA3F):c.1139G>A (p.Arg380His)	SEMA3F (R281H +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3358115	NM_004186.5(SEMA3F):c.871G>A (p.Ala291Thr)	SEMA3F (A192T +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3358089	NM_004186.5(SEMA3F):c.1860C>T (p.Ser620=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3358047	NM_004186.5(SEMA3F):c.880G>A (p.Ala294Thr)	SEMA3F (A195T +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3357984	NM_004186.5(SEMA3F):c.496G>A (p.Gly166Ser)	SEMA3F (G166S)	Single nucleotide variant (missense variant +1 more)	SEMA3F-related disorder	GUncertain significance
Select item 3357936	NM_004186.5(SEMA3F):c.2134A>G (p.Met712Val)	SEMA3F (M613V +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3357672	NM_004186.5(SEMA3F):c.1232C>T (p.Thr411Met)	SEMA3F (T312M +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3357624	NM_004186.5(SEMA3F):c.850G>A (p.Ala284Thr)	SEMA3F (A185T +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3357618	NM_004186.5(SEMA3F):c.429C>T (p.Thr143=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3357572	NM_004186.5(SEMA3F):c.1254G>A (p.Thr418=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3357454	NM_004186.5(SEMA3F):c.156C>T (p.Leu52=)	SEMA3F	Single nucleotide variant (5 prime UTR variant +1 more)	SEMA3F-related disorder	GLikely benign
Select item 3357451	NM_004186.5(SEMA3F):c.2093G>T (p.Gly698Val)	SEMA3F (G599V +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3357321	NM_004186.5(SEMA3F):c.981G>A (p.Pro327=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3356998	NM_004186.5(SEMA3F):c.1302C>T (p.Phe434=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3356891	NM_004186.5(SEMA3F):c.2172G>T (p.Thr724=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3356763	NM_004186.5(SEMA3F):c.610G>A (p.Asp204Asn)	SEMA3F (D105N +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3356757	NM_004186.5(SEMA3F):c.139T>C (p.Phe47Leu)	SEMA3F (F47L)	Single nucleotide variant (5 prime UTR variant +1 more)	SEMA3F-related disorder	GUncertain significance
Select item 3356657	NM_004186.5(SEMA3F):c.1075T>C (p.Phe359Leu)	SEMA3F (F260L +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3356498	NM_004186.5(SEMA3F):c.1155G>A (p.Gly385=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3356438	NM_004186.5(SEMA3F):c.1068C>T (p.Tyr356=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3356393	NM_004186.5(SEMA3F):c.112+6_112+8del	SEMA3F	Microsatellite (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3356277	NM_004186.5(SEMA3F):c.1948-6C>T	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3356029	NM_004186.5(SEMA3F):c.2292C>G (p.Pro764=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3356022	NM_004186.5(SEMA3F):c.1863A>C (p.Ala621=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3355999	NM_004186.5(SEMA3F):c.666G>A (p.Val222=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3355965	NM_004186.5(SEMA3F):c.22C>T (p.Leu8Phe)	SEMA3F (L8F)	Single nucleotide variant (missense variant +1 more)	SEMA3F-related disorder	GUncertain significance
Select item 3355879	NM_004186.5(SEMA3F):c.1928C>T (p.Pro643Leu)	SEMA3F (P544L +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3355862	NM_004186.5(SEMA3F):c.1426G>A (p.Gly476Arg)	SEMA3F (G377R +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3355854	NM_004186.5(SEMA3F):c.1818C>T (p.Asn606=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3355498	NM_004186.5(SEMA3F):c.457-10G>A	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3355480	NM_004186.5(SEMA3F):c.1465A>G (p.Thr489Ala)	SEMA3F (T390A +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3355472	NM_004186.5(SEMA3F):c.*9G>A	SEMA3F	Single nucleotide variant (3 prime UTR variant)	SEMA3F-related disorder	GLikely benign
Select item 3355409	NM_004186.5(SEMA3F):c.2338C>T (p.His780Tyr)	SEMA3F (H681Y +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3354952	NM_004186.5(SEMA3F):c.1089-10A>T	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3354937	NM_004186.5(SEMA3F):c.1281T>C (p.Tyr427=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3354752	NM_004186.5(SEMA3F):c.753G>C (p.Arg251=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3354739	NM_004186.5(SEMA3F):c.1915T>C (p.Phe639Leu)	SEMA3F (F540L +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3354710	NM_004186.5(SEMA3F):c.672C>T (p.Ile224=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3354674	NM_004186.5(SEMA3F):c.268C>T (p.Leu90Phe)	SEMA3F (L22F +1 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3354518	NM_004186.5(SEMA3F):c.959C>T (p.Ala320Val)	SEMA3F (A221V +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3354300	NM_004186.5(SEMA3F):c.113-10C>G	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3354188	NM_004186.5(SEMA3F):c.1674C>T (p.Cys558=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3354010	NM_004186.5(SEMA3F):c.1746-9C>T	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3354009	NM_004186.5(SEMA3F):c.906C>T (p.Asn302=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3353941	NM_004186.5(SEMA3F):c.422T>C (p.Met141Thr)	SEMA3F (M141T +1 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3353879	NM_004186.5(SEMA3F):c.1937G>A (p.Arg646Gln)	SEMA3F (R547Q +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3353851	NM_004186.5(SEMA3F):c.-10C>T	SEMA3F	Single nucleotide variant (5 prime UTR variant +1 more)	SEMA3F-related disorder	GLikely benign
Select item 3353783	NM_004186.5(SEMA3F):c.2167C>A (p.Pro723Thr)	SEMA3F (P624T +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3353542	NM_004186.5(SEMA3F):c.623A>C (p.Asp208Ala)	SEMA3F (D109A +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3353497	NM_004186.5(SEMA3F):c.2142C>T (p.Ala714=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3353381	NM_004186.5(SEMA3F):c.1093G>A (p.Val365Met)	SEMA3F (V266M +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3353301	NM_004186.5(SEMA3F):c.165C>T (p.Thr55=)	SEMA3F	Single nucleotide variant (5 prime UTR variant +1 more)	SEMA3F-related disorder	GLikely benign
Select item 3352557	NM_004186.5(SEMA3F):c.978C>T (p.Val326=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3352348	NM_004186.5(SEMA3F):c.838C>T (p.Arg280Cys)	SEMA3F (R181C +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3352148	NM_004186.5(SEMA3F):c.861G>A (p.Pro287=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3352094	NM_004186.5(SEMA3F):c.1366C>T (p.Arg456Cys)	SEMA3F (R357C +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3351974	NM_004186.5(SEMA3F):c.2251C>T (p.Arg751Cys)	SEMA3F (R652C +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3351875	NM_004186.5(SEMA3F):c.2333G>A (p.Arg778His)	SEMA3F (R679H +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3351848	NM_004186.5(SEMA3F):c.1612G>A (p.Val538Met)	SEMA3F (V439M +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3351819	NM_004186.5(SEMA3F):c.1546-5T>C	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3351760	NM_004186.5(SEMA3F):c.872C>T (p.Ala291Val)	SEMA3F (A192V +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3351740	NM_004186.5(SEMA3F):c.849G>A (p.Ser283=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3351679	NM_004186.5(SEMA3F):c.299G>A (p.Arg100His)	SEMA3F (R100H +1 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3351408	NM_004186.5(SEMA3F):c.315G>A (p.Val105=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3351377	NM_004186.5(SEMA3F):c.523C>T (p.Arg175Cys)	SEMA3F (R175C)	Single nucleotide variant (missense variant +1 more)	SEMA3F-related disorder	GUncertain significance
Select item 3351269	NM_004186.5(SEMA3F):c.752G>A (p.Arg251Gln)	SEMA3F (R152Q +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3351072	NM_004186.5(SEMA3F):c.1365C>T (p.Val455=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3351031	NM_004186.5(SEMA3F):c.312C>T (p.Cys104=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3350740	NM_004186.5(SEMA3F):c.2084A>G (p.His695Arg)	SEMA3F (H596R +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3350699	NM_004186.5(SEMA3F):c.494G>A (p.Arg165His)	SEMA3F (R165H)	Single nucleotide variant (missense variant +1 more)	SEMA3F-related disorder	GUncertain significance
Select item 3350651	NM_004186.5(SEMA3F):c.2013C>T (p.Ser671=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3350618	NM_004186.5(SEMA3F):c.544C>T (p.Arg182Cys)	SEMA3F (R182C)	Single nucleotide variant (missense variant +1 more)	SEMA3F-related disorder	GUncertain significance
Select item 3350601	NM_004186.5(SEMA3F):c.1947+8C>T	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3350586	NM_004186.5(SEMA3F):c.210C>T (p.Tyr70=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3350572	NM_004186.5(SEMA3F):c.138C>T (p.His46=)	SEMA3F	Single nucleotide variant (5 prime UTR variant +1 more)	SEMA3F-related disorder	GLikely benign
Select item 3350437	NM_004186.5(SEMA3F):c.2072G>A (p.Arg691Gln)	SEMA3F (R592Q +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3350421	NM_004186.5(SEMA3F):c.1089-3C>T	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GUncertain significance
Select item 3350381	NM_004186.5(SEMA3F):c.2349G>A (p.Pro783=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3350379	NM_004186.5(SEMA3F):c.1997G>A (p.Arg666His)	SEMA3F (R567H +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3350357	NM_004186.5(SEMA3F):c.1402G>A (p.Val468Met)	SEMA3F (V369M +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3350293	NM_004186.5(SEMA3F):c.1367G>A (p.Arg456His)	SEMA3F (R357H +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3350251	NM_004186.5(SEMA3F):c.1828G>A (p.Val610Met)	SEMA3F (V511M +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3350073	NM_004186.5(SEMA3F):c.2001A>G (p.Ala667=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3350010	NM_004186.5(SEMA3F):c.912C>T (p.Asp304=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3349975	NM_004186.5(SEMA3F):c.1195C>T (p.Pro399Ser)	SEMA3F (P300S +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3349298	NM_004186.5(SEMA3F):c.549+1G>A	SEMA3F	Single nucleotide variant (intron variant +1 more)	SEMA3F-related disorder	GUncertain significance
Select item 3349192	NM_004186.5(SEMA3F):c.904-7C>A	SEMA3F	Single nucleotide variant (intron variant)	SEMA3F-related disorder	GLikely benign
Select item 3349153	NM_004186.5(SEMA3F):c.931G>T (p.Val311Phe)	SEMA3F (V212F +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3349087	NM_004186.5(SEMA3F):c.1960G>A (p.Asp654Asn)	SEMA3F (D555N +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3349081	NM_004186.5(SEMA3F):c.703C>T (p.Arg235Cys)	SEMA3F (R136C +2 more)	Single nucleotide variant (missense variant)	SEMA3F-related disorder	GUncertain significance
Select item 3348978	NM_004186.5(SEMA3F):c.633G>A (p.Ser211=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign
Select item 3348838	NM_004186.5(SEMA3F):c.495C>G (p.Arg165=)	SEMA3F	Single nucleotide variant (synonymous variant +1 more)	SEMA3F-related disorder	GLikely benign
Select item 3348833	NM_004186.5(SEMA3F):c.648G>A (p.Glu216=)	SEMA3F	Single nucleotide variant (synonymous variant)	SEMA3F-related disorder	GLikely benign

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