"Genome-Nilou Lab"[submitter] AND "DNAJC6"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1258041	NM_001256864.2(DNAJC6):c.194-21G>T	DNAJC6	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1260451	NM_001256864.2(DNAJC6):c.194-20_194-19insG	DNAJC6	Insertion (intron variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign/Likely benign
Select item 1178033	NM_001256864.2(DNAJC6):c.194-6del	DNAJC6	Deletion (intron variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1277678	NM_001256864.2(DNAJC6):c.194-19T>G	DNAJC6	Single nucleotide variant (intron variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1215186	NM_001256864.2(DNAJC6):c.194-18T>G	DNAJC6	Single nucleotide variant (intron variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign/Likely benign
Select item 474676	NM_001256864.2(DNAJC6):c.194-5G>T	DNAJC6	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 663145	NM_001256864.2(DNAJC6):c.397A>T (p.Met133Leu)	DNAJC6 (M63L +2 more)	Single nucleotide variant (missense variant)	Juvenile onset Parkinson disease 19A +1 more	GUncertain significance
Select item 1170298	NM_001256864.2(DNAJC6):c.544-9C>T	DNAJC6	Single nucleotide variant (intron variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 474681	NM_001256864.2(DNAJC6):c.678G>A (p.Ala226=)	DNAJC6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 541544	NM_001256864.2(DNAJC6):c.745A>G (p.Ile249Val)	DNAJC6 (I249V +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1298426	NM_001256864.2(DNAJC6):c.829G>A (p.Ala277Thr)	DNAJC6 (A207T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 976692	NM_001256864.2(DNAJC6):c.988C>T (p.Arg330Ter)	DNAJC6 (R260* +2 more)	Single nucleotide variant (nonsense)	Juvenile onset Parkinson disease 19A	GPathogenic
Select item 623687	NM_001256864.2(DNAJC6):c.1039A>G (p.Ile347Val)	DNAJC6 (I277V +2 more)	Single nucleotide variant (missense variant)	Juvenile onset Parkinson disease 19A +2 more	GUncertain significance
Select item 1176504	NM_001256864.2(DNAJC6):c.1070T>C (p.Met357Thr)	DNAJC6 (M287T +2 more)	Single nucleotide variant (missense variant)	Juvenile onset Parkinson disease 19A +2 more	GUncertain significance
Select item 702187	NM_001256864.2(DNAJC6):c.1320A>T (p.Thr440=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign/Likely benign
Select item 445731	NM_001256864.2(DNAJC6):c.1456C>T (p.Leu486Phe)	DNAJC6 (L416F +2 more)	Single nucleotide variant (missense variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign/Likely benign
Select item 1170299	NM_001256864.2(DNAJC6):c.1500G>A (p.Glu500=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1167136	NM_001256864.2(DNAJC6):c.1506C>T (p.His502=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1418472	NM_001256864.2(DNAJC6):c.1646C>T (p.Pro549Leu)	DNAJC6 (P492L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 703807	NM_001256864.2(DNAJC6):c.1710G>A (p.Pro570=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign/Likely benign
Select item 623688	NM_001256864.2(DNAJC6):c.1817A>C (p.His606Pro)	DNAJC6 (H536P +2 more)	Single nucleotide variant (missense variant)	Juvenile onset Parkinson disease 19A +1 more	GUncertain significance
Select item 1522190	NM_001256864.2(DNAJC6):c.1832C>T (p.Ala611Val)	DNAJC6 (A611V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2053413	NM_001256864.2(DNAJC6):c.1841A>G (p.Gln614Arg)	DNAJC6 (Q614R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1167137	NM_001256864.2(DNAJC6):c.1983T>C (p.Ser661=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1170300	NM_001256864.2(DNAJC6):c.2010A>C (p.Pro670=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1376516	NM_001256864.2(DNAJC6):c.2072A>G (p.Asp691Gly)	DNAJC6 (D634G +2 more)	Single nucleotide variant (missense variant)	Juvenile onset Parkinson disease 19A +1 more	GUncertain significance
Select item 1196512	NM_001256864.2(DNAJC6):c.2159C>T (p.Ser720Leu)	DNAJC6 (S650L +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 1167138	NM_001256864.2(DNAJC6):c.2183G>A (p.Ser728Asn)	DNAJC6 (S658N +2 more)	Single nucleotide variant (missense variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1943951	NM_001256864.2(DNAJC6):c.2309C>T (p.Ala770Val)	DNAJC6 (A713V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 861071	NM_001256864.2(DNAJC6):c.2468G>A (p.Arg823His)	DNAJC6 (R823H +2 more)	Single nucleotide variant (missense variant)	Juvenile onset Parkinson disease 19A +1 more	GUncertain significance
Select item 1694517	NM_001256864.2(DNAJC6):c.2526A>G (p.Leu842=)	DNAJC6	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1416440	NM_001256864.2(DNAJC6):c.2715G>C (p.Glu905Asp)	DNAJC6 (E835D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1407142	NM_001256864.2(DNAJC6):c.2762A>T (p.Gln921Leu)	DNAJC6 (Q864L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

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Items: 33