"PreventionGenetics, part of Exact Sciences"[submitter] AND "CSNK1D"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053133	NM_004207.4(SLC16A3):c.*990G>A	CSNK1D, SLC16A3	Single nucleotide variant (3 prime UTR variant)	CSNK1D-related disorder	GLikely benign
Select item 3041815	NM_004207.4(SLC16A3):c.*1066A>G	CSNK1D, SLC16A3	Single nucleotide variant (synonymous variant +1 more)	CSNK1D-related disorder	GLikely benign
Select item 3048437	NM_001893.6(CSNK1D):c.1198-7C>T	CSNK1D	Single nucleotide variant (intron variant)	CSNK1D-related disorder	GLikely benign
Select item 3057884	NM_001893.6(CSNK1D):c.996C>G (p.Gly332=)	CSNK1D	Single nucleotide variant (synonymous variant +1 more)	CSNK1D-related disorder	GLikely benign
Select item 3040908	NM_001893.6(CSNK1D):c.864C>T (p.Phe288=)	CSNK1D	Single nucleotide variant (synonymous variant +1 more)	CSNK1D-related disorder	GLikely benign
Select item 3035264	NM_001893.6(CSNK1D):c.828G>A (p.Leu276=)	CSNK1D	Single nucleotide variant (synonymous variant +1 more)	CSNK1D-related disorder	GLikely benign

ClinVar