List of variants reported as uncertain significance for Spinocerebellar ataxia type 6

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.6001C>T (p.Pro2001Ser)	rs751947412	0.00006
NM_001127222.2(CACNA1A):c.6400C>T (p.Arg2134Cys)	rs121908235	0.00006
NM_001127222.2(CACNA1A):c.6368G>C (p.Arg2123Pro)	rs1220294928	0.00002
NM_001127222.2(CACNA1A):c.7067C>T (p.Thr2356Met)	rs780098532	0.00002
NM_001127222.2(CACNA1A):c.3149T>C (p.Ile1050Thr)	rs2057414053	0.00001
NM_001127222.2(CACNA1A):c.1583T>C (p.Leu528Pro)	rs2145030753
NM_001127222.2(CACNA1A):c.3006_3008del (p.Arg1004del)	rs763302316
NM_001127222.2(CACNA1A):c.3310_3315dup (p.Gly1104_Pro1105dup)	rs776584949
NM_001127222.2(CACNA1A):c.4009G>T (p.Asp1337Tyr)	rs1568473283
NM_001127222.2(CACNA1A):c.4297C>T (p.Arg1433Trp)	rs1275025158
NM_001127222.2(CACNA1A):c.5139T>A (p.Phe1713Leu)	rs2144646945
NM_001127222.2(CACNA1A):c.5651T>A (p.Val1884Asp)	rs2144595194
NM_001127222.2(CACNA1A):c.7087C>T (p.Arg2363Cys)
NM_001127222.2(CACNA1A):c.709A>G (p.Ile237Val)	rs2059190094

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