Individual ID: 28867142.28

Individual ID	28867142.28
Pubmed ID	28867142
Whose mosaic mutation	Male Patient
Origin of mosaic mutation in patients	de novo
Phenotypic Category	3
Disease	Autism Spectrum Disorders(view all the variants in this disease)
OMIM ID	209850

Variants

Found 10 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
1183	498	ATP5A1	18	43669564	43669564	Autism Spectrum Disorders	NextSeq500 v2
1184	506	ATP5B	12	57033938	57033938	Autism Spectrum Disorders	NextSeq500 v2
1214	10693	CCT6B	17	33266705	33266705	Autism Spectrum Disorders	NextSeq500 v2
1539	27131	SNX5	20	17930778	17930778	Autism Spectrum Disorders	NextSeq500 v2
29736	547	KIF1A	2	241724471	241724471	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29737	728294	D2HGDH	2	242684178	242684178	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29738	10752	CHL1	3	386367	386367	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29739	79885	HDAC11	3	13522828	13522828	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29740	152273	FGD5	3	14960293	14960293	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29802	51314	NME8	7	37889860	37889860	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500