ClinVar Miner

List of variants in gene DNAJC6 studied for Parkinson disease

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_001256864.2(DNAJC6):c.1039A>G (p.Ile347Val) rs200712827
NM_001256864.2(DNAJC6):c.1456C>T (p.Leu486Phe) rs78141380
NM_001256864.2(DNAJC6):c.170G>T (p.Arg57Leu)
NM_001256864.2(DNAJC6):c.175A>G (p.Ser59Gly)
NM_001256864.2(DNAJC6):c.194-5G>T rs753576283
NM_001256864.2(DNAJC6):c.2025G>T (p.Ser675=) rs185245369
NM_001256864.2(DNAJC6):c.2086T>C (p.Trp696Arg) rs1462099424
NM_001256864.2(DNAJC6):c.2223A>T (p.Thr741=) rs879255554
NM_001256864.2(DNAJC6):c.2290C>T (p.Leu764Phe) rs917235831
NM_001256864.2(DNAJC6):c.2468G>C (p.Arg823Pro)
NM_001256864.2(DNAJC6):c.2536C>T (p.Gln846Ter) rs886039854
NM_001256864.2(DNAJC6):c.2779A>G (p.Arg927Gly) rs879255630
NM_001256864.2(DNAJC6):c.2838C>T (p.Tyr946=) rs148209150
NM_001256864.2(DNAJC6):c.397A>T (p.Met133Leu)
NM_001256864.2(DNAJC6):c.678G>A (p.Ala226=) rs61753391
NM_001256864.2(DNAJC6):c.745A>G (p.Ile249Val) rs149588872
NM_001256864.2(DNAJC6):c.801-2A>G rs398122404
NM_001256864.2(DNAJC6):c.833A>G (p.Asp278Gly) rs368290134
NM_001256864.2(DNAJC6):c.996-9T>C rs187965193
NM_001256865.1(DNAJC6):c.2018-3T>C
NM_001256865.1(DNAJC6):c.2200C>T (p.Gln734Ter) rs398122405
NM_001256865.1(DNAJC6):c.244C>T (p.Arg82Ter) rs864622011

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