List of variants reported as pathogenic for striatonigral degeneration

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_018052.5(VAC14):c.1271G>T (p.Trp424Leu)	rs762388639	0.00001
NC_012920.1(MT-ATP6):m.8851T>C	rs199476136
NC_012920.1(MT-ATP6):m.9176T>C	rs199476135
NM_001385079.1(PDE10A):c.1696T>C (p.Phe566Leu)	rs875989841
NM_001385079.1(PDE10A):c.1798T>C (p.Phe600Leu)	rs875989840
NM_001385079.1(PDE10A):c.1799T>G (p.Phe600Cys)	rs1554258695
NM_003719.5(PDE8B):c.304G>T (p.Glu102Ter)	rs878853158
NM_003719.5(PDE8B):c.79del (p.Arg27fs)	rs878853157
NM_003719.5(PDE8B):c.94_95delinsC (p.Val32fs)	rs2149371451
NM_016553.5(NUP62):c.1172A>C (p.Gln391Pro)	rs121917865
NM_018052.5(VAC14):c.1528+1G>A	rs879255555
NM_018052.5(VAC14):c.1744G>T (p.Ala582Ser)	rs749094914
NM_018052.5(VAC14):c.1748C>T (p.Ser583Leu)	rs879255645

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