Individual ID: 28867142.36

Individual ID	28867142.36
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
1191	285237	C3ORF38	3	88205377	88205377	Autism Spectrum Disorders	NextSeq500 v2
1263		ELL2	5	95234143	95234143	Autism Spectrum Disorders	NextSeq500 v2
1424	23499	MACF1	1	39903616	39903616	Autism Spectrum Disorders	NextSeq500 v2
1490	24145	PANX1	11	93913089	93913089	Autism Spectrum Disorders	NextSeq500 v2
1536	9389	SLC22A14	3	38349069	38349069	Autism Spectrum Disorders	NextSeq500 v2
29776	83697	SLC4A9	5	139750705	139750705	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29777	3340	NDST1	5	149912558	149912558	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29778	2566	GABRG2	5	161524765	161524765	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29779	6586	SLIT3	5	168678421	168678421	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29780	153222	CREBRF	5	172550144	172550144	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29806	1278	COL1A2	7	94042413	94042413	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500