Related gene-specific medical variations for Gene (Select 8727) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270134	NM_003798.4(CTNNAL1):c.1778T>A (p.Ile593Asn)	CTNNAL1, LOC126860724 (I593N)	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 2395960	NM_003798.4(CTNNAL1):c.1767G>C (p.Gln589His)	CTNNAL1, LOC126860724 (Q589H)	Single nucleotide variant (missense variant)	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 2286910	NM_003798.4(CTNNAL1):c.1646T>A (p.Leu549Gln)	CTNNAL1, LOC126860724 (L549Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284257	NM_003798.4(CTNNAL1):c.1694T>C (p.Ile565Thr)	CTNNAL1, LOC126860724 (I565T)	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