Variant information


Systematic Name
(NM_004992.3:)		 c.467A>C
Protein name
(NP_004983)		 p.Asp156Ala
Alternate systematic Name
(NM_001110792.1:)		 c.503A>C
Alternate Protein name
(NP_001104262)		 p.(Asp168Ala)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296812T>G
Mutation type missense
Domain MBD
Pathogenicity Unknown

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.467A>C p.Asp156Ala Female Rett syndrome-classical 3625 Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms:Fukuda, T., Yamashita, Y., Nagamitsu, S., Miyamoto, K., Jin, J.-J., Ohmori, I., Ohtsuka, Y., Kuwajima, K., Endo, S., Iwai, T., Yamagata, H., Tabara, Y., Miki, T., Matsuishi, T., Kondo, I.:Brain & Development: 15737703 View details