Individual ID: 28867142.17

Individual ID	28867142.17
Pubmed ID	28867142
Whose mosaic mutation	Female 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
1549		SYNGAP1	6	33411384	33411384	Autism Spectrum Disorders	NextSeq500 v2
1575	57578	UNC79	14	94129046	94129046	Autism Spectrum Disorders	NextSeq500 v2
29717	89886	SLAMF9	1	159922117	159922117	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29876	253959	RALGAPA1	14	36207803	36207803	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29877	10175	CNIH1	14	54897061	54897061	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29878	23002	DAAM1	14	59791152	59791152	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29879	55218	EXD2	14	69701564	69701564	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29880	55640	FLVCR2	14	76045663	76045663	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29881	9369	NRXN3	14	79434627	79434627	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29882	79890	RIN3	14	93081784	93081784	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29883	5641	LGMN	14	93170685	93170685	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500