ClinVar for MedGen (Select 400169) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3764046	NM_004082.5(DCTN1):c.3114C>G (p.Asn1038Lys)	DCTN1 (N1001K +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3763846	NM_004082.5(DCTN1):c.18G>A (p.Arg6=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3763825	NM_004082.5(DCTN1):c.129T>C (p.Thr43=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3763755	NM_004082.5(DCTN1):c.362G>A (p.Gly121Glu)	DCTN1 (G104E +1 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3763198	NM_004082.5(DCTN1):c.2185-6C>T	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3763102	NM_004082.5(DCTN1):c.2060G>T (p.Ser687Ile)	DCTN1 (S553I +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3762896	NM_004082.5(DCTN1):c.1015T>C (p.Leu339=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3762793	NM_004082.5(DCTN1):c.844-19A>C	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3762524	NM_004082.5(DCTN1):c.2481C>T (p.Leu827=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3762405	NM_004082.5(DCTN1):c.2344C>T (p.Leu782Phe)	DCTN1 (L648F +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3762389	NM_004082.5(DCTN1):c.3518G>T (p.Arg1173Leu)	DCTN1 (R1034L +7 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3762356	NM_004082.5(DCTN1):c.1221A>G (p.Gln407=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3762054	NM_004082.5(DCTN1):c.352A>G (p.Lys118Glu)	DCTN1 (K101E +1 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3761835	NM_004082.5(DCTN1):c.3346-16_3346-14del	DCTN1	Microsatellite (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3761791	NM_004082.5(DCTN1):c.3610-10C>T	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3761508	NM_004082.5(DCTN1):c.2672A>G (p.Gln891Arg)	DCTN1 (Q757R +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3761482	NM_004082.5(DCTN1):c.415-12A>G	DCTN1 (M1V)	Single nucleotide variant (missense variant +2 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3761457	NM_004082.5(DCTN1):c.371C>A (p.Thr124Lys)	DCTN1 (T107K +1 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3761332	NM_004082.5(DCTN1):c.393+18G>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3761230	NM_004082.5(DCTN1):c.1983C>T (p.Ser661=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3761080	NM_004082.5(DCTN1):c.588C>G (p.Ile196Met)	DCTN1 (I159M +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3760908	NM_004082.5(DCTN1):c.2352C>T (p.Leu784=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3760890	NM_004082.5(DCTN1):c.596C>T (p.Pro199Leu)	DCTN1 (P162L +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3760860	NM_004082.5(DCTN1):c.1393-17A>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3760804	NM_004082.5(DCTN1):c.101A>G (p.Glu34Gly)	DCTN1 (E17G +1 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3760716	NM_004082.5(DCTN1):c.3498G>T (p.Thr1166=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3760608	NM_004082.5(DCTN1):c.1855-20C>T	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3759577	NM_004082.5(DCTN1):c.1855-16G>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3759496	NM_004082.5(DCTN1):c.1287+4T>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3759031	NM_004082.5(DCTN1):c.2354G>T (p.Arg785Leu)	DCTN1 (R651L +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3759030	NM_004082.5(DCTN1):c.2158C>T (p.Leu720Phe)	DCTN1 (L586F +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3759029	NM_004082.5(DCTN1):c.2515G>T (p.Ala839Ser)	DCTN1 (A705S +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3758943	NM_004082.5(DCTN1):c.1548C>T (p.Thr516=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3758820	NM_004082.5(DCTN1):c.1668_1673del (p.Ile557_Lys558del)	DCTN1	Deletion (inframe_deletion +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3758774	NM_004082.5(DCTN1):c.1128-19C>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3758700	NM_004082.5(DCTN1):c.255T>C (p.His85=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3758677	NM_004082.5(DCTN1):c.3700-14T>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3758674	NM_004082.5(DCTN1):c.3389A>G (p.His1130Arg)	DCTN1 (H1088R +7 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3758666	NM_004082.5(DCTN1):c.432+12T>C	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3758618	NM_004082.5(DCTN1):c.2831A>C (p.Lys944Thr)	DCTN1 (K810T +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3758510	NM_004082.5(DCTN1):c.594G>A (p.Thr198=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3758470	NM_004082.5(DCTN1):c.34-11G>C	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3758115	NM_004082.5(DCTN1):c.2628G>A (p.Gln876=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3757964	NM_004082.5(DCTN1):c.2868G>A (p.Lys956=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3757953	NM_004082.5(DCTN1):c.2121C>T (p.His707=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3757500	NM_004082.5(DCTN1):c.2902G>C (p.Glu968Gln)	DCTN1 (E834Q +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3757231	NM_004082.5(DCTN1):c.2930A>G (p.Glu977Gly)	DCTN1 (E843G +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3757216	NM_004082.5(DCTN1):c.3298A>C (p.Met1100Leu)	DCTN1 (M1058L +7 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3757122	NM_004082.5(DCTN1):c.2015+17del	DCTN1	Deletion (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3756990	NM_004082.5(DCTN1):c.3813G>T (p.Gln1271His)	DCTN1 (Q1132H +7 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756964	NM_004082.5(DCTN1):c.3349G>A (p.Ala1117Thr)	DCTN1 (A1075T +7 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756681	NM_004082.5(DCTN1):c.1128-6C>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3756677	NM_004082.5(DCTN1):c.2976G>T (p.Glu992Asp)	DCTN1 (E858D +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756627	NM_004082.5(DCTN1):c.878A>C (p.Tyr293Ser)	DCTN1 (Y159S +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756464	NM_004082.5(DCTN1):c.163G>A (p.Gly55Ser)	DCTN1 (G38S +1 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756345	NM_004082.5(DCTN1):c.347T>C (p.Val116Ala)	DCTN1 (V116A +1 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756277	NM_004082.5(DCTN1):c.433-19G>T	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3756104	NM_004082.5(DCTN1):c.1701+9A>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756053	NM_004082.5(DCTN1):c.2285T>C (p.Val762Ala)	DCTN1 (V628A +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756018	NM_004082.5(DCTN1):c.1854+2T>C	DCTN1	Single nucleotide variant (splice donor variant)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3756002	NM_004082.5(DCTN1):c.856G>T (p.Ala286Ser)	DCTN1 (A152S +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3755975	NM_004082.5(DCTN1):c.2760+5G>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3755790	NM_004082.5(DCTN1):c.3030-11C>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3755667	NM_004082.5(DCTN1):c.2317-4G>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3755635	NM_004082.5(DCTN1):c.2948C>A (p.Ala983Asp)	DCTN1 (A849D +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3755554	NM_004082.5(DCTN1):c.2824G>A (p.Gly942Ser)	DCTN1 (G808S +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3755378	NM_004082.5(DCTN1):c.844-20C>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3755293	NM_004082.5(DCTN1):c.1565A>G (p.Gln522Arg)	DCTN1 (Q388R +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3755149	NM_004082.5(DCTN1):c.2556T>A (p.Ile852=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3755097	NM_004082.5(DCTN1):c.3346-20C>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3755047	NM_004082.5(DCTN1):c.1363C>T (p.Arg455Cys)	DCTN1 (R321C +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3754675	NM_004082.5(DCTN1):c.2316+19C>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3754474	NM_004082.5(DCTN1):c.3211+10C>T	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3754389	NM_004082.5(DCTN1):c.348C>G (p.Val116=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3753574	NM_004082.5(DCTN1):c.3143T>C (p.Leu1048Pro)	DCTN1 (L1011P +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3753492	NM_004082.5(DCTN1):c.2241T>C (p.Ala747=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3753318	NM_004082.5(DCTN1):c.1766C>T (p.Thr589Ile)	DCTN1 (T455I +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3753155	NM_004082.5(DCTN1):c.3371C>T (p.Ala1124Val)	DCTN1 (A1082V +7 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3752889	NM_004082.5(DCTN1):c.79C>T (p.Leu27=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3752679	NM_004082.5(DCTN1):c.165C>G (p.Gly55=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3752498	NM_004082.5(DCTN1):c.1060G>A (p.Ala354Thr)	DCTN1 (A220T +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3752307	NM_004082.5(DCTN1):c.1902G>A (p.Glu634=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3751808	NM_004082.5(DCTN1):c.2848A>G (p.Thr950Ala)	DCTN1 (T816A +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3751758	NM_004082.5(DCTN1):c.400C>G (p.Leu134Val)	DCTN1 (L117V +1 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3751615	NM_004082.5(DCTN1):c.1393-10G>A	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3751606	NM_004082.5(DCTN1):c.3223G>A (p.Gly1075Arg)	DCTN1 (G1033R +7 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3751580	NM_004082.5(DCTN1):c.2521C>G (p.Leu841Val)	DCTN1 (L707V +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3751247	NM_004082.5(DCTN1):c.1877C>T (p.Ala626Val)	DCTN1 (A492V +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3751050	NM_004082.5(DCTN1):c.3699+18G>T	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3750982	NM_004082.5(DCTN1):c.1468G>T (p.Asp490Tyr)	DCTN1 (D356Y +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3750866	NM_004082.5(DCTN1):c.2317-9C>T	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3750855	NM_004082.5(DCTN1):c.3509A>G (p.Asp1170Gly)	DCTN1 (D1031G +7 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3750630	NM_004082.5(DCTN1):c.3346-16C>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3750562	NM_004082.5(DCTN1):c.2760+9A>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3750494	NM_004082.5(DCTN1):c.996G>C (p.Val332=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3750057	NM_004082.5(DCTN1):c.2317-9C>G	DCTN1	Single nucleotide variant (intron variant)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign
Select item 3750044	NM_004082.5(DCTN1):c.2873C>T (p.Ser958Leu)	DCTN1 (S824L +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3750036	NM_004082.5(DCTN1):c.2197A>G (p.Ile733Val)	DCTN1 (I599V +6 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3750030	NM_004082.5(DCTN1):c.268C>T (p.Arg90Cys)	DCTN1 (R73C +1 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GUncertain significance
Select item 3749864	NM_004082.5(DCTN1):c.3315C>T (p.Ser1105=)	DCTN1	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 1 +2 more	GLikely benign

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