Individual ID: 28867142.13

Individual ID	28867142.13
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
1225	64581	CLEC7A	12	10280034	10280034	Autism Spectrum Disorders	NextSeq500 v2
1242	29119	CTNNA3	10	69366755	69366755	Autism Spectrum Disorders	NextSeq500 v2
1410	58508	KMT2C	7	151836804	151836804	Autism Spectrum Disorders	NextSeq500 v2
1542	23524	SRRM2	16	2818164	2818164	Autism Spectrum Disorders	NextSeq500 v2
1550		SYT15	10	46968675	46968675	Autism Spectrum Disorders	NextSeq500 v2
1562	116447	TOP1MT	8	144397947	144397947	Autism Spectrum Disorders	NextSeq500 v2
29714	9557	CHD1L	1	146728216	146728216	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29847	28971	AAMDC	11	77580840	77580840	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29848	24145	PANX1	11	93913089	93913089	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29849	143884	CWF19L2	11	107300102	107300102	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29850	23085	ERC1	12	1345953	1345953	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500