List of variants in gene combination LOC130059440, TMEM231 reported as uncertain significance for cerebellar ataxia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001077418.3(TMEM231):c.140-33C>T	rs901311435	0.00004
NM_001077418.3(TMEM231):c.166G>C (p.Glu56Gln)	rs771783989	0.00002
NM_001077418.3(TMEM231):c.140-10T>C	rs2151710900
NM_001077418.3(TMEM231):c.140-33C>G	rs901311435
NM_001077418.3(TMEM231):c.140-39G>A
NM_001077418.3(TMEM231):c.144T>G (p.Phe48Leu)	rs2151710882
NM_001077418.3(TMEM231):c.155G>A (p.Arg52Gln)
NM_001077418.3(TMEM231):c.164A>G (p.Tyr55Cys)

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