"PreventionGenetics, part of Exact Sciences"[submitter] AND "CSNK2B"[g - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051024	NM_001320.7(CSNK2B):c.-1G>C	CSNK2B	Single nucleotide variant (5 prime UTR variant)	CSNK2B-related condition	GLikely benign
Select item 3048258	NM_001320.7(CSNK2B):c.6C>T (p.Ser2=)	CSNK2B	Single nucleotide variant (synonymous variant)	CSNK2B-related condition	GLikely benign
Select item 520596	NM_001320.7(CSNK2B):c.94G>A (p.Asp32Asn)	CSNK2B (D32N)	Single nucleotide variant (missense variant)	Poirier-Bienvenu neurodevelopmental syndrome +4 more	GConflicting classifications of pathogenicity
Select item 426599	NM_001320.7(CSNK2B):c.139C>T (p.Arg47Ter)	CSNK2B (R47*)	Single nucleotide variant (nonsense)	not provided +3 more	GPathogenic
Select item 2628412	NM_001320.7(CSNK2B):c.175+1G>A	CSNK2B	Single nucleotide variant (splice donor variant)	CSNK2B-related condition	GLikely pathogenic
Select item 3053440	NM_001320.7(CSNK2B):c.252C>T (p.His84=)	CSNK2B	Single nucleotide variant (synonymous variant)	CSNK2B-related condition	GLikely benign
Select item 3053867	NM_001320.7(CSNK2B):c.292T>C (p.Leu98=)	CSNK2B	Single nucleotide variant (synonymous variant)	CSNK2B-related condition	GLikely benign
Select item 3052733	NM_001320.7(CSNK2B):c.462G>A (p.Thr154=)	CSNK2B	Single nucleotide variant (synonymous variant)	CSNK2B-related condition	GLikely benign
Select item 2631763	NM_001320.7(CSNK2B):c.505A>G (p.Met169Val)	CSNK2B (M166V +1 more)	Single nucleotide variant (missense variant)	CSNK2B-related condition	GUncertain significance
Select item 3050546	NM_001320.7(CSNK2B):c.639G>A (p.Thr213=)	CSNK2B	Single nucleotide variant (synonymous variant)	CSNK2B-related condition	GLikely benign