ClinVar Miner

List of variants in gene VPS35 studied for Parkinson disease 17

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Total variants: 70
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HGVS dbSNP
NM_018206.6(VPS35):c.*161C>T
NM_018206.6(VPS35):c.*276A>C rs886052009
NM_018206.6(VPS35):c.*283C>A
NM_018206.6(VPS35):c.*289C>T
NM_018206.6(VPS35):c.*345T>G
NM_018206.6(VPS35):c.*346G>A rs545755034
NM_018206.6(VPS35):c.*34A>G
NM_018206.6(VPS35):c.*354G>C rs572048744
NM_018206.6(VPS35):c.*380G>A rs886052004
NM_018206.6(VPS35):c.*401G>A rs553790361
NM_018206.6(VPS35):c.*422C>A
NM_018206.6(VPS35):c.*575A>T
NM_018206.6(VPS35):c.*617A>G rs746602580
NM_018206.6(VPS35):c.-19C>T rs573920049
NM_018206.6(VPS35):c.-35C>G
NM_018206.6(VPS35):c.-35C>T rs189775907
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.1268C>T (p.Pro423Leu)
NM_018206.6(VPS35):c.1290C>T (p.Tyr430=)
NM_018206.6(VPS35):c.1313G>A (p.Cys438Tyr) rs745893720
NM_018206.6(VPS35):c.1317T>C (p.Tyr439=)
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.1488T>C (p.His496=) rs776877370
NM_018206.6(VPS35):c.151G>A (p.Gly51Ser) rs193077277
NM_018206.6(VPS35):c.1520A>T (p.Tyr507Phe) rs1555465749
NM_018206.6(VPS35):c.1525-5G>T
NM_018206.6(VPS35):c.1550T>G (p.Phe517Cys) rs1567264486
NM_018206.6(VPS35):c.1570C>T (p.Arg524Trp) rs184277092
NM_018206.6(VPS35):c.1679T>C (p.Ile560Thr) rs760128592
NM_018206.6(VPS35):c.171G>A (p.Met57Ile) rs183554824
NM_018206.6(VPS35):c.1796A>G (p.His599Arg) rs1434487321
NM_018206.6(VPS35):c.1809A>T (p.Ala603=)
NM_018206.6(VPS35):c.1819A>G (p.Met607Val) rs1555523076
NM_018206.6(VPS35):c.1858G>A (p.Asp620Asn) rs188286943
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.1900A>G (p.Thr634Ala)
NM_018206.6(VPS35):c.1912A>T (p.Met638Leu) rs144997996
NM_018206.6(VPS35):c.1938= (p.His646=) rs168745
NM_018206.6(VPS35):c.1938C>T (p.His646=)
NM_018206.6(VPS35):c.2073C>T (p.His691=)
NM_018206.6(VPS35):c.2145A>G (p.Leu715=) rs145033509
NM_018206.6(VPS35):c.2210C>T (p.Ala737Val) rs749516404
NM_018206.6(VPS35):c.2211+11T>C
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.2353G>C (p.Glu785Gln)
NM_018206.6(VPS35):c.2359G>A (p.Glu787Lys) rs777050595
NM_018206.6(VPS35):c.505G>C (p.Asp169His)
NM_018206.6(VPS35):c.506+4A>C
NM_018206.6(VPS35):c.648G>A (p.Leu216=)
NM_018206.6(VPS35):c.678C>T (p.Arg226=) rs376845827
NM_018206.6(VPS35):c.723T>G (p.Ile241Met) rs192783364
NM_018206.6(VPS35):c.851G>A (p.Arg284Gln) rs771276024
NM_018206.6(VPS35):c.89T>A (p.Met30Lys) rs145147781
NM_018206.6(VPS35):c.915-3del rs569369937
NM_018206.6(VPS35):c.945A>T (p.Gly315=) rs144346159
NM_018206.6(VPS35):c.946C>T (p.Pro316Ser) rs770029606
NM_018206.6(VPS35):c.959C>T (p.Ala320Val) rs747944333
NM_018206.6(VPS35):c.993G>T (p.Gln331His)

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