Related gene-specific medical variations for Gene (Select 8853) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2495815	NM_003887.3(ASAP2):c.1267A>G (p.Ile423Val)	ASAP2, LOC126806133 (I423V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2249292	NM_003887.3(ASAP2):c.1292C>T (p.Thr431Met)	ASAP2, LOC126806133 (T431M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 767783	NM_003887.3(ASAP2):c.1302C>T (p.Asp434=)	ASAP2, LOC126806133	Single nucleotide variant (synonymous variant)	not provided	GBenign

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