ClinVar Miner

List of variants in gene VPS35 reported as likely benign for Parkinson disease 17

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_018206.6(VPS35):c.*289C>T
NM_018206.6(VPS35):c.*34A>G
NM_018206.6(VPS35):c.-35C>T rs189775907
NM_018206.6(VPS35):c.1020A>G (p.Gln340=) rs188883365
NM_018206.6(VPS35):c.1317T>C (p.Tyr439=)
NM_018206.6(VPS35):c.1881C>T (p.Ala627=) rs138794859
NM_018206.6(VPS35):c.2145A>G (p.Leu715=) rs145033509
NM_018206.6(VPS35):c.2241C>T (p.Ile747=) rs140543776
NM_018206.6(VPS35):c.678C>T (p.Arg226=) rs376845827
NM_018206.6(VPS35):c.945A>T (p.Gly315=) rs144346159

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