List of variants in gene AKT1 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001382430.1(AKT1):c.47-319T>C	rs2498793	0.01863
NM_001382430.1(AKT1):c.288-321C>T	rs143245295	0.01703
NM_001382430.1(AKT1):c.703-125G>A	rs3730328	0.01676
NM_001382430.1(AKT1):c.567+14G>A	rs3730345	0.01364
NM_001382430.1(AKT1):c.1260+190C>T	rs61761245	0.01309
NM_001382430.1(AKT1):c.176-261G>A	rs61761184	0.01270
NM_001382430.1(AKT1):c.1261-196C>T	rs118098425	0.01089
NM_001382430.1(AKT1):c.1251C>T (p.Tyr417=)	rs139297659	0.01031
NM_001382430.1(AKT1):c.1260+93C>T	rs150861537	0.01009
NM_001382430.1(AKT1):c.1172+207C>T	rs144246504	0.00992
NM_001382430.1(AKT1):c.1172+71G>A	rs35622471	0.00899
NM_001382430.1(AKT1):c.288-121G>A	rs141074179	0.00886
NM_001382430.1(AKT1):c.1179C>T (p.Gly393=)	rs11555434	0.00832
NM_001382430.1(AKT1):c.1173-89C>T	rs149990267	0.00548
NM_001382430.1(AKT1):c.176-245C>A	rs190333080	0.00493
NM_001382430.1(AKT1):c.702+102G>A	rs61761197	0.00380
NM_001382430.1(AKT1):c.-45C>G	rs34757714
NM_001382430.1(AKT1):c.957+3G>A	rs1219173005

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