Individual ID: 23101622.01

Individual ID	23101622.01
Pubmed ID	23101622
Whose mosaic mutation	Patient
Phenotypic Category	3
Disease	Hemimegalencephaly(view all the variants in this disease)
OMIM ID	611223

Variants

Found 2 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
91	10000	AKT3	1	243859016	243859016	Hemimegalencephaly	Sanger
92	10000	AKT3	1	243859016	243859016	Hemimegalencephaly	Sanger