Related gene-specific medical variations for Gene (Select 54942) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3131574	NM_017832.4(ABITRAM):c.5C>T (p.Ala2Val)	ABITRAM, LOC130002307 (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078641	NM_003798.4(CTNNAL1):c.1950C>G (p.Asp650Glu)	ABITRAM, CTNNAL1 (D650E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3078639	NM_003798.4(CTNNAL1):c.1913C>T (p.Thr638Ile)	ABITRAM, CTNNAL1 (T638I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559155	NM_003798.4(CTNNAL1):c.1994C>T (p.Pro665Leu)	ABITRAM, CTNNAL1 (P665L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348579	NM_003798.4(CTNNAL1):c.1996C>G (p.Leu666Val)	ABITRAM, CTNNAL1 (L666V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250280	NM_003798.4(CTNNAL1):c.1922T>G (p.Val641Gly)	ABITRAM, CTNNAL1 (V641G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204605	NM_003798.4(CTNNAL1):c.1909C>T (p.Leu637Phe)	ABITRAM, CTNNAL1 (L637F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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