ClinVar for Gene (Select 56920) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358847	NM_020163.3(SEMA3G):c.526C>T (p.Arg176Cys)	SEMA3G (R176C)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3358819	NM_020163.3(SEMA3G):c.324G>A (p.Lys108=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3358754	NM_020163.3(SEMA3G):c.387C>T (p.Thr129=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3358710	NM_020163.3(SEMA3G):c.36A>G (p.Leu12=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3358668	NM_020163.3(SEMA3G):c.1698C>T (p.His566=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3358613	NM_020163.3(SEMA3G):c.1467+3A>C	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3358607	NM_020163.3(SEMA3G):c.1271G>A (p.Arg424His)	SEMA3G (R424H)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3358565	NM_020163.3(SEMA3G):c.803G>A (p.Arg268His)	SEMA3G (R268H)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3358556	NM_020163.3(SEMA3G):c.2236C>T (p.Arg746Trp)	SEMA3G (R746W)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3358474	NM_020163.3(SEMA3G):c.1865A>T (p.Glu622Val)	SEMA3G (E622V)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3358440	NM_020163.3(SEMA3G):c.773C>T (p.Ser258Leu)	SEMA3G (S258L)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3358179	NM_020163.3(SEMA3G):c.2046G>C (p.Leu682=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3358131	NM_020163.3(SEMA3G):c.1878+7G>A	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3358111	NM_020163.3(SEMA3G):c.774G>A (p.Ser258=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3358088	NM_020163.3(SEMA3G):c.1371G>A (p.Gly457=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3357985	NM_020163.3(SEMA3G):c.1673G>A (p.Arg558Gln)	SEMA3G (R558Q)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357965	NM_020163.3(SEMA3G):c.553G>A (p.Gly185Arg)	SEMA3G (G185R)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357733	NM_020163.3(SEMA3G):c.1912C>T (p.Arg638Trp)	SEMA3G (R638W)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357722	NM_020163.3(SEMA3G):c.2245_2259del (p.Gln749_Lys753del)	SEMA3G	Deletion (inframe_deletion)	SEMA3G-related disorder	GUncertain significance
Select item 3357703	NM_020163.3(SEMA3G):c.1879-10C>T	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3357694	NM_020163.3(SEMA3G):c.891C>G (p.Pro297=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3357625	NM_020163.3(SEMA3G):c.1002C>T (p.Ala334=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3357566	NM_020163.3(SEMA3G):c.*4G>C	SEMA3G	Single nucleotide variant (3 prime UTR variant)	SEMA3G-related disorder	GLikely benign
Select item 3357424	NM_020163.3(SEMA3G):c.115+5C>T	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3357399	NM_020163.3(SEMA3G):c.1576G>A (p.Gly526Ser)	SEMA3G (G526S)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357373	NM_020163.3(SEMA3G):c.1486G>A (p.Glu496Lys)	SEMA3G (E496K)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357315	NM_020163.3(SEMA3G):c.821C>G (p.Ala274Gly)	SEMA3G (A274G)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357306	NM_020163.3(SEMA3G):c.2114C>T (p.Ala705Val)	SEMA3G (A705V)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357251	NM_020163.3(SEMA3G):c.1218G>A (p.Gln406=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3357230	NM_020163.3(SEMA3G):c.218G>A (p.Gly73Asp)	SEMA3G (G73D)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357199	NM_020163.3(SEMA3G):c.245G>A (p.Arg82Gln)	SEMA3G (R82Q)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357194	NM_020163.3(SEMA3G):c.1652G>A (p.Arg551His)	SEMA3G (R551H)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3357005	NM_020163.3(SEMA3G):c.1699G>A (p.Gly567Ser)	SEMA3G (G567S)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3356911	NM_020163.3(SEMA3G):c.1041A>G (p.Ala347=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3356905	NM_020163.3(SEMA3G):c.1467+6C>A	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3356898	NM_020163.3(SEMA3G):c.1014C>T (p.Gly338=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3356690	NM_020163.3(SEMA3G):c.361C>A (p.Arg121=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3356672	NM_020163.3(SEMA3G):c.1935T>C (p.Leu645=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3356605	NM_020163.3(SEMA3G):c.1293C>T (p.His431=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3356432	NM_020163.3(SEMA3G):c.355T>C (p.Phe119Leu)	SEMA3G (F119L)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3356422	NM_020163.3(SEMA3G):c.1923G>C (p.Leu641=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3356332	NM_020163.3(SEMA3G):c.1923G>T (p.Leu641=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3356264	NM_020163.3(SEMA3G):c.1020C>T (p.Ala340=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3356144	NM_020163.3(SEMA3G):c.276+5G>C	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GUncertain significance
Select item 3356080	NM_020163.3(SEMA3G):c.550+7G>A	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3355952	NM_020163.3(SEMA3G):c.*2A>G	SEMA3G	Single nucleotide variant (3 prime UTR variant)	SEMA3G-related disorder	GLikely benign
Select item 3355868	NM_020163.3(SEMA3G):c.1527C>T (p.Gly509=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355841	NM_020163.3(SEMA3G):c.349G>A (p.Ala117Thr)	SEMA3G (A117T)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3355783	NM_020163.3(SEMA3G):c.244C>T (p.Arg82Trp)	SEMA3G (R82W)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3355775	NM_020163.3(SEMA3G):c.1908G>C (p.Thr636=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355773	NM_020163.3(SEMA3G):c.504G>A (p.Gly168=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355745	NM_020163.3(SEMA3G):c.309G>A (p.Glu103=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355719	NM_020163.3(SEMA3G):c.291G>A (p.Pro97=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355713	NM_020163.3(SEMA3G):c.180C>T (p.Ala60=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355683	NM_020163.3(SEMA3G):c.500G>A (p.Arg167Gln)	SEMA3G (R167Q)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3355438	NM_020163.3(SEMA3G):c.2133G>A (p.Leu711=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355374	NM_020163.3(SEMA3G):c.519G>A (p.Glu173=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355325	NM_020163.3(SEMA3G):c.2340G>C (p.Glu780Asp)	SEMA3G (E780D)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3355296	NM_020163.3(SEMA3G):c.1878+8A>T	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3355072	NM_020163.3(SEMA3G):c.1668G>A (p.Lys556=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3355053	NM_020163.3(SEMA3G):c.1510-6C>T	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3355044	NM_020163.3(SEMA3G):c.272G>T (p.Arg91Leu)	SEMA3G (R91L)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3355028	NM_020163.3(SEMA3G):c.1263A>C (p.Arg421=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3354912	NM_020163.3(SEMA3G):c.260G>A (p.Trp87Ter)	SEMA3G (W87*)	Single nucleotide variant (nonsense)	SEMA3G-related disorder	GUncertain significance
Select item 3354905	NM_020163.3(SEMA3G):c.2134C>A (p.Gln712Lys)	SEMA3G (Q712K)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3354696	NM_020163.3(SEMA3G):c.500G>C (p.Arg167Pro)	SEMA3G (R167P)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3354575	NM_020163.3(SEMA3G):c.958G>C (p.Gly320Arg)	SEMA3G (G320R)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3354558	NM_020163.3(SEMA3G):c.1480A>G (p.Ile494Val)	SEMA3G (I494V)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3354503	NM_020163.3(SEMA3G):c.537C>G (p.Ala179=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3354488	NM_020163.3(SEMA3G):c.182T>C (p.Met61Thr)	SEMA3G (M61T)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3354384	NM_020163.3(SEMA3G):c.2286G>A (p.Lys762=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3354351	NM_020163.3(SEMA3G):c.471C>T (p.His157=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3354234	NM_020163.3(SEMA3G):c.364G>T (p.Val122Leu)	SEMA3G (V122L)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3354200	NM_020163.3(SEMA3G):c.1509+3A>G	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3354100	NM_020163.3(SEMA3G):c.1187G>A (p.Ser396Asn)	SEMA3G (S396N)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3354091	NM_020163.3(SEMA3G):c.610C>T (p.Arg204Ter)	SEMA3G (R204*)	Single nucleotide variant (nonsense)	SEMA3G-related disorder	GUncertain significance
Select item 3354089	NM_020163.3(SEMA3G):c.1467+7A>C	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3353991	NM_020163.3(SEMA3G):c.156C>T (p.Pro52=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353952	NM_020163.3(SEMA3G):c.1926C>T (p.Phe642=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353901	NM_020163.3(SEMA3G):c.417C>T (p.Phe139=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353775	NM_020163.3(SEMA3G):c.1281T>C (p.Leu427=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353720	NM_020163.3(SEMA3G):c.1097A>G (p.Gln366Arg)	SEMA3G (Q366R)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3353658	NM_020163.3(SEMA3G):c.1284C>T (p.Val428=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353422	NM_020163.3(SEMA3G):c.1879-4G>C	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3353420	NM_020163.3(SEMA3G):c.78C>T (p.Pro26=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353390	NM_020163.3(SEMA3G):c.228C>T (p.Asp76=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353341	NM_020163.3(SEMA3G):c.237C>T (p.Tyr79=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353339	NM_020163.3(SEMA3G):c.1104G>A (p.Gly368=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353305	NM_020163.3(SEMA3G):c.1917G>A (p.Gly639=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3353278	NM_020163.3(SEMA3G):c.1035C>A (p.His345Gln)	SEMA3G (H345Q)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3353276	NM_020163.3(SEMA3G):c.1123C>T (p.Pro375Ser)	SEMA3G (P375S)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3353271	NM_020163.3(SEMA3G):c.702G>T (p.Glu234Asp)	SEMA3G (E234D)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3352569	NM_020163.3(SEMA3G):c.115+7G>A	SEMA3G	Single nucleotide variant (intron variant)	SEMA3G-related disorder	GLikely benign
Select item 3352525	NM_020163.3(SEMA3G):c.1575C>T (p.Tyr525=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GUncertain significance
Select item 3352328	NM_020163.3(SEMA3G):c.1895G>A (p.Arg632Gln)	SEMA3G (R632Q)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3352265	NM_020163.3(SEMA3G):c.2325G>A (p.Thr775=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3352168	NM_020163.3(SEMA3G):c.2185G>A (p.Val729Met)	SEMA3G (V729M)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3352031	NM_020163.3(SEMA3G):c.45C>G (p.Leu15=)	SEMA3G	Single nucleotide variant (synonymous variant)	SEMA3G-related disorder	GLikely benign
Select item 3351885	NM_020163.3(SEMA3G):c.2183G>A (p.Arg728His)	SEMA3G (R728H)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance
Select item 3351766	NM_020163.3(SEMA3G):c.1651C>T (p.Arg551Cys)	SEMA3G (R551C)	Single nucleotide variant (missense variant)	SEMA3G-related disorder	GUncertain significance

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