List of variants in gene AKT3 reported as benign for central nervous system malformation

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_005465.7(AKT3):c.1416C>G (p.Ser472=)	rs148332912	0.00352
NM_005465.7(AKT3):c.1359T>C (p.Asp453=)	rs142844303	0.00141
NM_005465.7(AKT3):c.285-13C>T	rs201603638	0.00051
NM_005465.7(AKT3):c.807C>T (p.Tyr269=)	rs150205993	0.00044
NM_005465.7(AKT3):c.792C>T (p.Ser264=)	rs77764554	0.00039
NM_005465.7(AKT3):c.46+12G>A	rs184404650	0.00036
NM_005465.7(AKT3):c.1398G>A (p.Pro466=)	rs150573714	0.00015
NM_005465.7(AKT3):c.1163+16C>T	rs781443210	0.00002
NM_005465.7(AKT3):c.1044C>T (p.Asn348=)	rs199771220	0.00001
NM_005465.7(AKT3):c.1251+15T>C
NM_005465.7(AKT3):c.173-23_173-20del	rs773557899
NM_005465.7(AKT3):c.430-17dup	rs780927904
NM_005465.7(AKT3):c.46+11C>T
NM_005465.7(AKT3):c.628-9dup

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