"PreventionGenetics, part of Exact Sciences"[submitter] AND "CBX2"[gen - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043499	NM_005189.3(CBX2):c.267C>T (p.Cys89=)	CBX2	Single nucleotide variant (synonymous variant)	CBX2-related condition	GLikely benign
Select item 2634053	NM_005189.3(CBX2):c.288+52G>T	CBX2 (V114L)	Single nucleotide variant (missense variant +1 more)	CBX2-related condition	GUncertain significance
Select item 708978	NM_005189.3(CBX2):c.342G>A (p.Thr114=)	CBX2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 784364	NM_005189.3(CBX2):c.577C>A (p.Leu193Met)	CBX2 (L193M)	Single nucleotide variant (missense variant)	CBX2-related condition +1 more	GBenign
Select item 2061244	NM_005189.3(CBX2):c.669C>T (p.Gly223=)	CBX2	Single nucleotide variant (synonymous variant)	CBX2-related condition +1 more	GLikely benign
Select item 3037754	NM_005189.3(CBX2):c.1125C>T (p.Ala375=)	CBX2	Single nucleotide variant (synonymous variant)	CBX2-related condition	GLikely benign
Select item 3049157	NM_005189.3(CBX2):c.1128C>T (p.Thr376=)	CBX2	Single nucleotide variant (synonymous variant)	CBX2-related condition	GLikely benign
Select item 1559855	NM_005189.3(CBX2):c.1146G>A (p.Pro382=)	CBX2	Single nucleotide variant (synonymous variant)	CBX2-related condition +1 more	GLikely benign
Select item 1663234	NM_005189.3(CBX2):c.1401G>A (p.Ser467=)	CBX2	Single nucleotide variant (synonymous variant)	CBX2-related condition +1 more	GLikely benign
Select item 3051861	NM_005189.3(CBX2):c.1428G>T (p.Pro476=)	CBX2	Single nucleotide variant (synonymous variant)	CBX2-related condition	GLikely benign