Individual ID: 28867142.30

Individual ID	28867142.30
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
1232	1288	COL4A6	X	107414663	107414663	Autism Spectrum Disorders	NextSeq500 v2
1374	2534	FYN	6	112015899	112015899	Autism Spectrum Disorders	NextSeq500 v2
1480	10392	NOD1	7	30486597	30486597	Autism Spectrum Disorders	NextSeq500 v2
1519	5511	PPP1R8	1	28169828	28169828	Autism Spectrum Disorders	NextSeq500 v2
1537	6586	SLIT3	5	168678421	168678421	Autism Spectrum Disorders	NextSeq500 v2
29746	4134	MAP4	3	47918907	47918907	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29747	389170	LEKR1	3	156570593	156570593	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29748	151827	LRRC34	3	169513985	169513985	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29749	1962	EHHADH	3	184910031	184910031	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29750	9076	CLDN1	3	190030680	190030680	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29803	3092	HIP1	7	75177092	75177092	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500