List of variants in gene CPAP reported as likely benign for Seckel syndrome 4

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_018451.5(CPAP):c.646T>C (p.Cys216Arg)	rs143260721	0.00148
NM_018451.5(CPAP):c.656C>T (p.Pro219Leu)	rs139844197	0.00140
NM_018451.5(CPAP):c.2298T>A (p.Asp766Glu)	rs79951875	0.00096
NM_018451.5(CPAP):c.2571C>G (p.Ser857Arg)	rs78628025	0.00094

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