Related gene-specific medical variations for Gene (Select 1453) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3356244	NM_001363749.2(CSNK1D):c.1249C>T (p.Arg417Cys)	CSNK1D, SLC16A3 (R417C)	Single nucleotide variant (missense variant +1 more)	CSNK1D-related disorder	GLikely benign
Select item 3053133	NC_000017.11:g.82239966G>A	CSNK1D, SLC16A3	Single nucleotide variant (3 prime UTR variant)	CSNK1D-related disorder	GLikely benign
Select item 3041815	NM_001363749.2(CSNK1D):c.1218T>C (p.Ser406=)	CSNK1D, SLC16A3	Single nucleotide variant (synonymous variant +1 more)	CSNK1D-related disorder	GLikely benign

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