Proband information


Proband id 1912
Systematic Name
(NM_004992.3:)		 c.1446C>T
Protein name
(NP_004983)		 p.Thr482Thr
Alternate systematic Name
(NM_001110792.1:)		 c.1482C>T
Alternate Protein name
(NP_001104262)		 p.(=)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153295833G>A
Mutation type Silent
Domain C-term
Pathogenicity Silent polymorphism
Evidence of Pathogenicity
Detection Direct sequencing or DHPLC
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 Not known
Phenotype-class Rett syndrome-Not certain
Reference :::

Matching entries in the proband database


No: Systematic Name Protein name Gender Carrier result Phenotype Proband id Reference
1 c.1446C>T p.Thr482Thr Female Rett syndrome-Not certain 1912 :::