Proband information


Proband id 2460
Systematic Name
(NM_004992.3:)		 c.[710G>T(;)763C>T]
Protein name
(NP_004983)		 p.[Gly237Val(;)Arg255*]
Alternate systematic Name
(NM_001110792.1:)		 c.[746G>T;799C>T]
Alternate Protein name
(NP_001104262)		 p.?
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.[153296569C>A;153296516G>A]
Mutation type missense, nonsense
Domain TRD
Pathogenicity Mutation associated with disease
Evidence of Pathogenicity 100 chromosomes tested and not found in 100 chromosomes
Detection Direct
Extent Exons 2-4
Source of DNA Blood
Carrier N
Carrier result
Other mutations N
X-inactivation results
X-inactivation relatives
Gender Female
Sporadic/Familial Sporadic
Phenotype-class Rett syndrome-Classical
Reference :::

Matching entries in the proband database


No: Systematic Name Protein name Gender Carrier result Phenotype Proband id Reference
1 c.[710G>T(;)763C>T] p.[Gly237Val(;)Arg255*] Female Rett syndrome-Classical 2460 :::