C4538355[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 259204	NM_003977.4(AIP):c.132C>T (p.Asp44=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +3 more	GBenign
Select item 305728	NM_003977.4(AIP):c.516C>T (p.Asp172=)	AIP	Single nucleotide variant (synonymous variant)	Somatotroph adenoma +2 more	GBenign
Select item 259205	NM_003977.4(AIP):c.682C>A (p.Gln228Lys)	AIP (Q228K +1 more)	Single nucleotide variant (missense variant)	Somatotroph adenoma +3 more	GBenign

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