List of variants in gene CEP164 reported as likely benign for not provided

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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_014956.5(CEP164):c.3716C>T (p.Pro1239Leu)	rs61995733	0.01531
NM_014956.5(CEP164):c.3225C>T (p.Thr1075=)	rs144421639	0.00210
NM_014956.5(CEP164):c.2772C>G (p.Leu924=)	rs117473319	0.00201
NM_014956.5(CEP164):c.1220C>T (p.Ser407Phe)	rs150314805	0.00084
NM_014956.5(CEP164):c.2244G>T (p.Leu748=)	rs1377025009	0.00031
NM_014956.5(CEP164):c.3364C>T (p.Arg1122Cys)	rs149875085	0.00008
NM_014956.5(CEP164):c.4106C>T (p.Pro1369Leu)	rs148116542	0.00006
NM_014956.5(CEP164):c.4265G>A (p.Arg1422His)	rs74653460	0.00004
NM_014956.5(CEP164):c.1815A>G (p.Gln605=)	rs1592325888	0.00001
NM_014956.5(CEP164):c.2526A>G (p.Glu842=)	rs1592370762
NM_014956.5(CEP164):c.3462C>G (p.Gly1154=)	rs1374201587
NM_014956.5(CEP164):c.380C>A (p.Pro127His)	rs143659874
NM_014956.5(CEP164):c.380C>T (p.Pro127Leu)	rs143659874
NM_014956.5(CEP164):c.3903C>T (p.Leu1301=)	rs1592512650
NM_014956.5(CEP164):c.4203C>A (p.Val1401=)	rs544976647
NM_014956.5(CEP164):c.4218C>T (p.Ser1406=)	rs1592531756
NM_014956.5(CEP164):c.468C>T (p.Thr156=)	rs771340026
NM_014956.5(CEP164):c.79C>A (p.Gln27Lys)	rs565845914

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