ClinVar Miner

List of variants studied for Parkinson disease 17 by Invitae

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Total variants: 28
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HGVS dbSNP
NM_018206.6(VPS35):c.1020A>G (p.Gln340=) rs188883365
NM_018206.6(VPS35):c.1035G>A (p.Glu345=) rs563975281
NM_018206.6(VPS35):c.1145A>G (p.Lys382Arg) rs116254156
NM_018206.6(VPS35):c.1151A>G (p.Asn384Ser)
NM_018206.6(VPS35):c.1290C>T (p.Tyr430=)
NM_018206.6(VPS35):c.1313G>A (p.Cys438Tyr) rs745893720
NM_018206.6(VPS35):c.1369-9A>G
NM_018206.6(VPS35):c.1371G>A (p.Val457=)
NM_018206.6(VPS35):c.1391T>C (p.Val464Ala) rs1555465774
NM_018206.6(VPS35):c.13C>T (p.Gln5Ter)
NM_018206.6(VPS35):c.1420C>G (p.Gln474Glu) rs370401767
NM_018206.6(VPS35):c.1480T>A (p.Phe494Ile)
NM_018206.6(VPS35):c.151G>A (p.Gly51Ser) rs193077277
NM_018206.6(VPS35):c.1550T>G (p.Phe517Cys) rs1567264486
NM_018206.6(VPS35):c.1881C>T (p.Ala627=) rs138794859
NM_018206.6(VPS35):c.1893C>T (p.Ile631=)
NM_018206.6(VPS35):c.1895T>C (p.Ile632Thr)
NM_018206.6(VPS35):c.1938= (p.His646=) rs168745
NM_018206.6(VPS35):c.1938C>T (p.His646=)
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.2320C>A (p.Leu774Met) rs192419029
NM_018206.6(VPS35):c.2350C>A (p.Pro784Thr)
NM_018206.6(VPS35):c.506+4A>C
NM_018206.6(VPS35):c.915-3del rs569369937
NM_018206.6(VPS35):c.945A>T (p.Gly315=) rs144346159
NM_018206.6(VPS35):c.959C>T (p.Ala320Val) rs747944333
NM_018206.6(VPS35):c.993G>T (p.Gln331His)

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