Related gene-specific medical variations for Gene (Select 51529) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3350262	NM_005782.4(ALYREF):c.46C>T (p.Leu16=)	ALYREF, ANAPC11	Single nucleotide variant (synonymous variant +2 more)	ALYREF-related disorder	GLikely benign
Select item 2636880	NM_005782.4(ALYREF):c.5C>A (p.Pro2His)	ALYREF, ANAPC11 (P2H)	Single nucleotide variant (missense variant +2 more)	ALYREF-related disorder	GUncertain significance
Select item 2279903	NM_005782.4(ALYREF):c.11C>T (p.Ser4Phe)	ALYREF, ANAPC11 (S4F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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