Individual ID: 28867142.26

Individual ID	28867142.26
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 11 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
1160	51412	ACTL6B	7	100252651	100252651	Autism Spectrum Disorders	NextSeq500 v2
1215	10693	CCT6B	17	33266705	33266705	Autism Spectrum Disorders	NextSeq500 v2
1235	50509	COL5A3	19	10092741	10092741	Autism Spectrum Disorders	NextSeq500 v2
1548	23345	SYNE1	6	152782817	152782817	Autism Spectrum Disorders	NextSeq500 v2
1578	55187	VPS13D	1	12428626	12428626	Autism Spectrum Disorders	NextSeq500 v2
29726	4703	NEB	2	152543981	152543981	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29727	29994	BAZ2B	2	160239207	160239207	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29728	6326	SCN2A	2	166211152	166211152	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29729	8647	ABCB11	2	169853212	169853212	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29730	7273	TTN	2	179605302	179605302	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29801	5137	PDE1C	7	31855578	31855578	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500