List of variants in gene CPAP reported as benign for Microcephaly 6, primary, autosomal recessive

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_018451.5(CPAP):c.3216+7A>G	rs9318917	0.80822
NM_018451.5(CPAP):c.3042A>G (p.Glu1014=)	rs3742165	0.47759
NM_018451.5(CPAP):c.2635T>G (p.Ser879Ala)	rs17402892	0.10073
NM_018451.5(CPAP):c.253C>A (p.Pro85Thr)	rs9511510	0.10060
NM_018451.5(CPAP):c.1560A>T (p.Thr520=)	rs17081368	0.04825
NM_018451.5(CPAP):c.163C>G (p.Pro55Ala)	rs17081389	0.02639
NM_018451.5(CPAP):c.187G>C (p.Asp63His)	rs7336216	0.02151
NM_018451.5(CPAP):c.1881G>A (p.Pro627=)	rs75985315	0.01708
NM_018451.5(CPAP):c.2031C>T (p.Ala677=)	rs61729909	0.01628
NM_018451.5(CPAP):c.287A>G (p.His96Arg)	rs61739263	0.01206
NM_018451.5(CPAP):c.68A>G (p.Asn23Ser)	rs116981543	0.00264
NM_018451.5(CPAP):c.61A>G (p.Met21Val)	rs35498994
NM_018451.5(CPAP):c.61A>T (p.Met21Leu)	rs35498994

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