"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "AK - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 221141	NM_001382430.1(AKT1):c.1251C>T (p.Tyr417=)	AKT1	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 240104	NM_001382430.1(AKT1):c.1227C>T (p.Ala409=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 473849	NM_001382430.1(AKT1):c.1194C>T (p.Asp398=)	AKT1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 240103	NM_001382430.1(AKT1):c.1179C>T (p.Gly393=)	AKT1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 220941	NM_001382430.1(AKT1):c.958-7C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GBenign
Select item 416469	NM_001382430.1(AKT1):c.604C>T (p.Leu202=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GBenign
Select item 416470	NM_001382430.1(AKT1):c.558C>T (p.Ile186=)	AKT1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

ClinVar