"Illumina Laboratory Services, Illumina"[submitter] AND "LRRK2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 369016	NM_198578.4(LRRK2):c.-124G>C	LRRK2, LOC130007688	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign/Likely benign
Select item 883497	NM_198578.4(LRRK2):c.-91C>T	LOC130007688, LRRK2	Single nucleotide variant (5 prime UTR variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 881128	NM_198578.4(LRRK2):c.-74C>A	LOC130007688, LRRK2	Single nucleotide variant (5 prime UTR variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 308609	NM_198578.4(LRRK2):c.-44G>A	LOC130007688, LRRK2	Single nucleotide variant (5 prime UTR variant)	Autosomal dominant Parkinson disease 8	GLikely benign
Select item 881129	NM_198578.4(LRRK2):c.102G>C (p.Thr34=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8 +1 more	GConflicting classifications of pathogenicity
Select item 533778	NM_198578.4(LRRK2):c.177T>A (p.Asn59Lys)	LRRK2 (N59K)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GConflicting classifications of pathogenicity
Select item 881130	NM_198578.4(LRRK2):c.215T>C (p.Met72Thr)	LRRK2 (M72T)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 881131	NM_198578.4(LRRK2):c.228T>C (p.Ser76=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 308610	NM_198578.4(LRRK2):c.344A>C (p.His115Pro)	LRRK2 (H115P)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 39167	NM_198578.4(LRRK2):c.356T>C (p.Leu119Pro)	LRRK2 (L119P)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 706229	NM_198578.4(LRRK2):c.364C>T (p.Leu122=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8 +2 more	GBenign/Likely benign
Select item 39192	NM_198578.4(LRRK2):c.457T>C (p.Leu153=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 881601	NM_198578.4(LRRK2):c.606C>T (p.Asn202=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 39223	NM_198578.4(LRRK2):c.632C>T (p.Ala211Val)	LRRK2 (A211V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 308611	NM_198578.4(LRRK2):c.709AAT[1] (p.Asn238del)	LRRK2 (N238del)	Microsatellite (inframe_deletion)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 586130	NM_198578.4(LRRK2):c.736A>C (p.Asn246His)	LRRK2 (N246H)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 804996	NM_198578.4(LRRK2):c.825T>C (p.His275=)	LRRK2	Single nucleotide variant (synonymous variant)	LRRK2-related condition +3 more	GConflicting classifications of pathogenicity
Select item 882756	NM_198578.4(LRRK2):c.839-4T>G	LRRK2	Single nucleotide variant (intron variant)	Autosomal dominant Parkinson disease 8	GConflicting classifications of pathogenicity
Select item 308612	NM_198578.4(LRRK2):c.867C>T (p.Asn289=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8 +1 more	GBenign/Likely benign
Select item 882757	NM_198578.4(LRRK2):c.921A>G (p.Ala307=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 39246	NM_198578.4(LRRK2):c.936G>T (p.Ala312=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8 +2 more	GBenign/Likely benign
Select item 39128	NM_198578.4(LRRK2):c.1000G>A (p.Glu334Lys)	LRRK2 (E334K)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 663402	NM_198578.4(LRRK2):c.1073C>T (p.Thr358Met)	LRRK2 (T358M)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GConflicting classifications of pathogenicity
Select item 308613	NM_198578.4(LRRK2):c.1102-10C>A	LRRK2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 308614	NM_198578.4(LRRK2):c.1182-4A>G	LRRK2	Single nucleotide variant (intron variant)	Autosomal dominant Parkinson disease 8 +1 more	GBenign/Likely benign
Select item 883550	NM_198578.4(LRRK2):c.1224T>G (p.His408Gln)	LRRK2 (H408Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 39131	NM_198578.4(LRRK2):c.1256C>T (p.Ala419Val)	LRRK2 (A419V)	Single nucleotide variant (missense variant)	LRRK2-related condition +2 more	GBenign/Likely benign
Select item 883551	NM_198578.4(LRRK2):c.1260T>C (p.Asn420=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 695715	NM_198578.4(LRRK2):c.1383T>C (p.Ser461=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +3 more	GLikely benign
Select item 308615	NM_198578.4(LRRK2):c.1446A>G (p.Ala482=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 883552	NM_198578.4(LRRK2):c.1473G>T (p.Met491Ile)	LRRK2 (M491I)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 722201	NM_198578.4(LRRK2):c.1476A>G (p.Lys492=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 39137	NM_198578.4(LRRK2):c.1561A>G (p.Arg521Gly)	LRRK2 (R521G)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 39139	NM_198578.4(LRRK2):c.1653C>G (p.Asn551Lys)	LRRK2 (N551K)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 881176	NM_198578.4(LRRK2):c.1655G>A (p.Arg552Lys)	LRRK2 (R552K)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GUncertain significance
Select item 881177	NM_198578.4(LRRK2):c.1656+6T>C	LRRK2	Single nucleotide variant (intron variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 308616	NM_198578.4(LRRK2):c.2070+9T>A	LRRK2	Single nucleotide variant (intron variant)	Autosomal dominant Parkinson disease 8	GConflicting classifications of pathogenicity
Select item 39146	NM_198578.4(LRRK2):c.2167A>G (p.Ile723Val)	LRRK2 (I723V)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 39148	NM_198578.4(LRRK2):c.2264C>T (p.Pro755Leu)	LRRK2 (P755L)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 881178	NM_198578.4(LRRK2):c.2282T>C (p.Leu761Ser)	LRRK2 (L761S)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GUncertain significance
Select item 39149	NM_198578.4(LRRK2):c.2378G>T (p.Arg793Met)	LRRK2 (R793M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 881644	NM_198578.4(LRRK2):c.2443C>A (p.Pro815Thr)	LRRK2 (P815T)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 308617	NM_198578.4(LRRK2):c.2501-9dup	LRRK2	Duplication (intron variant)	not provided +2 more	GBenign
Select item 881645	NM_198578.4(LRRK2):c.2579G>A (p.Ser860Asn)	LRRK2 (S860N)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GLikely benign
Select item 308618	NM_198578.4(LRRK2):c.2588A>G (p.Asn863Ser)	LRRK2 (N863S)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 705830	NM_198578.4(LRRK2):c.2594C>T (p.Ser865Phe)	LRRK2 (S865F)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 308619	NM_198578.4(LRRK2):c.2689+20dup	LRRK2	Duplication (intron variant)	Autosomal dominant Parkinson disease 8	GBenign/Likely benign
Select item 631544	NM_198578.4(LRRK2):c.2752C>T (p.Arg918Ter)	LRRK2 (R918*)	Single nucleotide variant (nonsense)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 881646	NM_198578.4(LRRK2):c.2758G>A (p.Ala920Thr)	LRRK2 (A920T)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GConflicting classifications of pathogenicity
Select item 308620	NM_198578.4(LRRK2):c.2826T>C (p.His942=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 39156	NM_198578.4(LRRK2):c.2857T>C (p.Leu953=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 881647	NM_198578.4(LRRK2):c.2864C>T (p.Ser955Leu)	LRRK2 (S955L)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GLikely benign
Select item 308621	NM_198578.4(LRRK2):c.2900A>G (p.His967Arg)	LRRK2 (H967R)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 308622	NM_198578.4(LRRK2):c.2987A>T (p.Asp996Val)	LRRK2 (D996V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 39159	NM_198578.4(LRRK2):c.3018A>G (p.Ile1006Met)	LRRK2 (I1006M)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 308623	NM_198578.4(LRRK2):c.3026A>C (p.His1009Pro)	LRRK2 (H1009P)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 39163	NM_198578.4(LRRK2):c.3333G>T (p.Gln1111His)	LRRK2 (Q1111H)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 308624	NM_198578.4(LRRK2):c.3429C>T (p.Ser1143=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 308625	NM_198578.4(LRRK2):c.3435A>C (p.Ser1145=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8 +1 more	GConflicting classifications of pathogenicity
Select item 767350	NM_198578.4(LRRK2):c.3496+9T>G	LRRK2	Single nucleotide variant (intron variant)	LRRK2-related condition +1 more	GBenign/Likely benign
Select item 308626	NM_198578.4(LRRK2):c.3497-8del	LRRK2	Deletion (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 308627	NM_198578.4(LRRK2):c.3595C>A (p.Arg1199=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 883595	NM_198578.4(LRRK2):c.3615C>G (p.Ser1205Arg)	LRRK2 (S1205R)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 308628	NM_198578.4(LRRK2):c.3678A>C (p.Leu1226Phe)	LRRK2 (L1226F)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 308629	NM_198578.4(LRRK2):c.3777+7C>T	LRRK2	Single nucleotide variant (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 308630	NM_198578.4(LRRK2):c.3778-9C>T	LRRK2	Single nucleotide variant (intron variant)	Autosomal dominant Parkinson disease 8 +1 more	GBenign/Likely benign
Select item 39173	NM_198578.4(LRRK2):c.3784C>G (p.Pro1262Ala)	LRRK2 (P1262A)	Single nucleotide variant (missense variant)	LRRK2-related condition +2 more	GBenign/Likely benign
Select item 308631	NM_198578.4(LRRK2):c.3864G>A (p.Met1288Ile)	LRRK2 (M1288I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 39174	NM_198578.4(LRRK2):c.3960G>T (p.Arg1320Ser)	LRRK2 (R1320S)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GLikely benign
Select item 308632	NM_198578.4(LRRK2):c.3969A>G (p.Gln1323=)	LRRK2	Single nucleotide variant (synonymous variant)	LRRK2-related condition +2 more	GConflicting classifications of pathogenicity
Select item 632191	NM_198578.4(LRRK2):c.4037del (p.Gly1346fs)	LRRK2 (G1346fs)	Deletion (frameshift variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 39176	NM_198578.4(LRRK2):c.4111A>G (p.Ile1371Val)	LRRK2 (I1371V)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 881230	NM_198578.4(LRRK2):c.4165G>A (p.Val1389Ile)	LRRK2 (V1389I)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GUncertain significance
Select item 39178	NM_198578.4(LRRK2):c.4193G>A (p.Arg1398His)	LRRK2 (R1398H)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 39179	NM_198578.4(LRRK2):c.4229C>T (p.Thr1410Met)	LRRK2 (T1410M)	Single nucleotide variant (missense variant)	LRRK2-related condition +2 more	GBenign/Likely benign
Select item 39181	NM_198578.4(LRRK2):c.4269G>A (p.Lys1423=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 881231	NM_198578.4(LRRK2):c.4317+3G>A	LRRK2	Single nucleotide variant (intron variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 308633	NM_198578.4(LRRK2):c.4317+12del	LRRK2	Deletion (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 39186	NM_198578.4(LRRK2):c.4337C>T (p.Pro1446Leu)	LRRK2 (P1446L)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GLikely benign
Select item 1199187	NM_198578.4(LRRK2):c.4453T>G (p.Tyr1485Asp)	LRRK2 (Y1485D)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 703922	NM_198578.4(LRRK2):c.4536+3A>G	LRRK2	Single nucleotide variant (intron variant)	Autosomal dominant Parkinson disease 8 +1 more	GConflicting classifications of pathogenicity
Select item 39191	NM_198578.4(LRRK2):c.4541G>A (p.Arg1514Gln)	LRRK2 (R1514Q)	Single nucleotide variant (missense variant)	LRRK2-related condition +2 more	GBenign/Likely benign
Select item 39193	NM_198578.4(LRRK2):c.4624C>T (p.Pro1542Ser)	LRRK2 (P1542S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 308634	NM_198578.4(LRRK2):c.4627A>G (p.Ile1543Val)	LRRK2 (I1543V)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 308635	NM_198578.4(LRRK2):c.4828-9A>T	LRRK2	Single nucleotide variant (intron variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 39197	NM_198578.4(LRRK2):c.4872C>A (p.Gly1624=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 39198	NM_198578.4(LRRK2):c.4883G>C (p.Arg1628Pro)	LRRK2 (R1628P)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 39199	NM_198578.4(LRRK2):c.4911A>G (p.Lys1637=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 308636	NM_198578.4(LRRK2):c.4930A>G (p.Asn1644Asp)	LRRK2 (N1644D)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GUncertain significance
Select item 308637	NM_198578.4(LRRK2):c.4934A>G (p.Tyr1645Cys)	LRRK2 (Y1645C)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 39200	NM_198578.4(LRRK2):c.4937T>C (p.Met1646Thr)	LRRK2 (M1646T)	Single nucleotide variant (missense variant)	LRRK2-related condition +2 more	GBenign/Likely benign
Select item 39201	NM_198578.4(LRRK2):c.4939T>A (p.Ser1647Thr)	LRRK2 (S1647T)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8 +1 more	GBenign
Select item 39202	NM_198578.4(LRRK2):c.4959A>G (p.Leu1653=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8 +1 more	GBenign/Likely benign
Select item 39203	NM_198578.4(LRRK2):c.5163A>G (p.Ser1721=)	LRRK2	Single nucleotide variant (synonymous variant)	Autosomal dominant Parkinson disease 8 +3 more	GBenign/Likely benign
Select item 308638	NM_198578.4(LRRK2):c.5270A>G (p.Asn1757Ser)	LRRK2 (N1757S)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 39209	NM_198578.4(LRRK2):c.5457T>C (p.Gly1819=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 308639	NM_198578.4(LRRK2):c.5510-9A>G	LRRK2	Single nucleotide variant (intron variant)	not provided +4 more	GBenign/Likely benign
Select item 39213	NM_198578.4(LRRK2):c.5606T>C (p.Met1869Thr)	LRRK2 (M1869T)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 308640	NM_198578.4(LRRK2):c.5713G>C (p.Val1905Leu)	LRRK2 (V1905L)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GConflicting classifications of pathogenicity
Select item 883636	NM_198578.4(LRRK2):c.5799A>T (p.Ile1933=)	LRRK2	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity

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