Individual ID: 28867142.20

Individual ID	28867142.20
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 10 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
1553	79718	TBL1XR1	3	176765107	176765107	Autism Spectrum Disorders	NextSeq500 v2
29900	51168	MYO15A	17	18039050	18039050	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29901	10693	CCT6B	17	33266705	33266705	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29902	26574	AATF	17	35413915	35413915	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29903	8396	PIP4K2B	17	36927464	36927464	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29904	3881	KRT31	17	39551197	39551197	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29905	124535	HSF5	17	56536222	56536222	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29906	85302	FBF1	17	73906883	73906883	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29907	3607	FOXK2	17	80559225	80559225	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29908	7525	YES1	18	756622	756622	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500