Individual ID: 28867142.18

Individual ID	28867142.18
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
1576	9958	USP15	12	62749154	62749154	Autism Spectrum Disorders	NextSeq500 v2
29708	23499	MACF1	1	39784265	39784265	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29718	59349	KLHL12	1	202880289	202880289	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29884	57578	UNC79	14	94129046	94129046	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29885	5330	PLCB2	15	40590077	40590077	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29886	23005	MAPKBP1	15	42116026	42116026	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29887	2200	FBN1	15	48717681	48717681	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29888	23312	DMXL2	15	51791966	51791966	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29889	1106	CHD2	15	93467760	93467760	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29890	123283	TARSL2	15	102242560	102242560	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29891	10921	RNPS1	16	2312406	2312406	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500