Individual ID: 28867142.37

Individual ID	28867142.37
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
1193	731	C8A	1	57347157	57347157	Autism Spectrum Disorders	NextSeq500 v2
1382		HEG1	3	124732716	124732716	Autism Spectrum Disorders	NextSeq500 v2
1504	54872	PIGG	4	499570	499570	Autism Spectrum Disorders	NextSeq500 v2
1526	5998	RGS3	9	116267745	116267745	Autism Spectrum Disorders	NextSeq500 v2
1557	7067	THRA	17	38243055	38243055	Autism Spectrum Disorders	NextSeq500 v2
1580	57705	WDFY4	10	49939237	49939237	Autism Spectrum Disorders	NextSeq500 v2
29781	56940	DUSP22	6	345911	345911	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29782	7407	VARS	6	31749930	31749930	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29783	117283	IP6K3	6	33694623	33694623	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29784	3159	HMGA1	6	34208681	34208681	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29785	340204	CLPSL1	6	35755695	35755695	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500