List of variants in gene AKT2 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001626.6(AKT2):c.93C>T (p.Ser31=)	rs35588791	0.00270
NM_001626.6(AKT2):c.945G>A (p.Glu315=)	rs150000674	0.00174
NM_001626.6(AKT2):c.442-8C>T	rs201884933	0.00059
NM_001626.6(AKT2):c.960+3G>A	rs56165898	0.00048
NM_001626.6(AKT2):c.1366+106A>G	rs187555784	0.00040
NM_001626.6(AKT2):c.1366+20G>A	rs375549081	0.00040
NM_001626.6(AKT2):c.711G>C (p.Leu237=)	rs776435289	0.00003
NM_001626.6(AKT2):c.1110G>T (p.Pro370=)	rs41309435
NM_001626.6(AKT2):c.125C>T (p.Pro42Leu)
NM_001626.6(AKT2):c.368A>C (p.Lys123Thr)	rs2514295922
NM_001626.6(AKT2):c.527G>A (p.Arg176His)
NM_001626.6(AKT2):c.531C>T (p.Tyr177=)	rs1974436210
NM_001626.6(AKT2):c.709-3C>G	rs370790932

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