CSNK1D[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3048437	NM_001893.6(CSNK1D):c.1198-7C>T	CSNK1D	Single nucleotide variant (intron variant)	CSNK1D-related disorder	GLikely benign
Select item 2648493	NM_001893.6(CSNK1D):c.1155C>T (p.Asp385=)	CSNK1D	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3078272	NM_001893.6(CSNK1D):c.1135G>A (p.Val379Ile)	CSNK1D (V379I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269879	NM_001893.6(CSNK1D):c.1055C>T (p.Thr352Met)	CSNK1D (T352M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3078271	NM_001893.6(CSNK1D):c.1024C>G (p.Pro342Ala)	CSNK1D (P342A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269878	NM_001893.6(CSNK1D):c.1010C>T (p.Thr337Met)	CSNK1D (T337M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
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 2527718	NM_001893.6(CSNK1D):c.932G>A (p.Arg311Gln)	CSNK1D (R311Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269880	NM_001893.6(CSNK1D):c.916C>T (p.Arg306Trp)	CSNK1D (R306W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 768923	NM_001893.6(CSNK1D):c.912C>T (p.Ala304=)	CSNK1D	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3239068	NM_001893.6(CSNK1D):c.910G>A (p.Ala304Thr)	CSNK1D (A304T)	Single nucleotide variant (missense variant +1 more)	not provided	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
Select item 2648494	NM_001893.6(CSNK1D):c.234C>T (p.Asn78=)	CSNK1D	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 773768	NM_001893.6(CSNK1D):c.213C>T (p.Cys71=)	CSNK1D	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 50319	NM_001893.6(CSNK1D):c.137A>G (p.His46Arg)	CSNK1D (H46R)	Single nucleotide variant (missense variant +1 more)	Advanced sleep phase syndrome 2	GPathogenic
Select item 8741	NM_001893.6(CSNK1D):c.130A>G (p.Thr44Ala)	CSNK1D (T44A)	Single nucleotide variant (missense variant +1 more)	Advanced sleep phase syndrome 2	GPathogenic
Select item 3269881	NM_001893.6(CSNK1D):c.89C>T (p.Ala30Val)	CSNK1D (A30V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance