PPP2CB[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2550507	NM_001009552.2(PPP2CB):c.859C>G (p.Leu287Val)	PPP2CB (L287V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303497	NM_001009552.2(PPP2CB):c.485A>G (p.Gln162Arg)	PPP2CB (Q162R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658518	NM_001009552.2(PPP2CB):c.480T>C (p.Asp160=)	PPP2CB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3217747	NM_001009552.2(PPP2CB):c.422A>T (p.Asn141Ile)	PPP2CB (N141I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217746	NM_001009552.2(PPP2CB):c.422A>G (p.Asn141Ser)	PPP2CB (N141S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262642	NM_001009552.2(PPP2CB):c.316C>T (p.Arg106Cys)	PPP2CB (R106C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456741	NM_001009552.2(PPP2CB):c.197T>C (p.Met66Thr)	PPP2CB (M66T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217745	NM_001009552.2(PPP2CB):c.142G>A (p.Val48Ile)	PPP2CB (V48I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217744	NM_001009552.2(PPP2CB):c.103G>A (p.Ala35Thr)	PPP2CB (A35T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248249	NM_001009552.2(PPP2CB):c.98A>G (p.Glu33Gly)	PPP2CB (E33G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487764	NM_001009552.2(PPP2CB):c.55G>A (p.Glu19Lys)	PPP2CB (E19K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance