Individual ID: 28867142.29

Individual ID	28867142.29
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
1168		ARMC9	2	232127057	232127057	Autism Spectrum Disorders	NextSeq500 v2
1244	143884	CWF19L2	11	107300102	107300102	Autism Spectrum Disorders	NextSeq500 v2
1404		KIAA0430	16	15690622	15690622	Autism Spectrum Disorders	NextSeq500 v2
1417		KRT39	17	39120763	39120763	Autism Spectrum Disorders	NextSeq500 v2
1572	7275	TUB	11	8122426	8122426	Autism Spectrum Disorders	NextSeq500 v2
1574		UBL4A	X	153713959	153713959	Autism Spectrum Disorders	NextSeq500 v2
29741	9940	DLEC1	3	38105382	38105382	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29742	9389	SLC22A14	3	38349069	38349069	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29743	6336	SCN10A	3	38770255	38770255	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29744	1499	CTNNB1	3	41274877	41274877	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29745	1232	CCR3	3	46307288	46307288	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500