List of variants in gene CERKL reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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: 8

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HGVS	dbSNP	gnomAD frequency
NM_201548.5(CERKL):c.313C>T (p.Arg105Trp)	rs149078111	0.00370
NM_201548.5(CERKL):c.783T>C (p.Pro261=)	rs77741297	0.00158
NM_201548.5(CERKL):c.735G>C (p.Leu245=)	rs140898616	0.00093
NM_201548.5(CERKL):c.1523C>T (p.Ser508Leu)	rs146913105	0.00076
NM_201548.5(CERKL):c.102G>T (p.Thr34=)	rs149346187	0.00034
NM_201548.5(CERKL):c.78C>T (p.Ala26=)	rs754384634	0.00006
NM_201548.5(CERKL):c.90G>A (p.Pro30=)	rs1213574692	0.00002
NM_201548.5(CERKL):c.906G>A (p.Gln302=)

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