List of variants in gene CC2D2A reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.2774G>A (p.Arg925Gln)	rs200707391	0.00061
NM_001378615.1(CC2D2A):c.541G>A (p.Val181Ile)	rs745646755	0.00003
NM_001378615.1(CC2D2A):c.517C>T (p.Arg173Ter)	rs386833763	0.00001
NM_001378615.1(CC2D2A):c.667G>A (p.Glu223Lys)	rs1471249662
NM_001378615.1(CC2D2A):c.740G>T (p.Gly247Val)	rs746210662

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