List of variants in gene CERKL reported as likely benign for perceptual disorders

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_201548.5(CERKL):c.677+566G>T	rs10185262	0.00821
NM_201548.5(CERKL):c.66C>G (p.Pro22=)	rs199762900	0.00287
NM_201548.5(CERKL):c.157G>A (p.Glu53Lys)	rs141389059	0.00238
NM_201548.5(CERKL):c.820+9G>A	rs189638090	0.00163
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.102G>T (p.Thr34=)	rs149346187	0.00034
NM_201548.5(CERKL):c.900T>C (p.His300=)	rs183252158	0.00020
NM_201548.5(CERKL):c.1127A>C (p.Gln376Pro)	rs746220721	0.00007
NM_201548.5(CERKL):c.327T>G (p.Val109=)	rs907281117	0.00007
NM_201548.5(CERKL):c.1159+8G>A	rs201778792	0.00004
NM_201548.5(CERKL):c.1466C>G (p.Thr489Ser)	rs768292284	0.00002
NM_201548.5(CERKL):c.933C>T (p.Thr311=)	rs371048058	0.00001
NM_201548.5(CERKL):c.1143G>A (p.Gln381=)	rs1574435800
NM_201548.5(CERKL):c.1449GGA[3] (p.Glu486del)
NM_201548.5(CERKL):c.264T>C (p.Cys88=)	rs765835624
NM_201548.5(CERKL):c.699T>C (p.Asp233=)	rs769255785

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