Proband information


Proband id 2142
Systematic Name
(NM_004992.3:)		 c.1404G>A
Protein name
(NP_004983)		 p.Arg468Arg
Alternate systematic Name
(NM_001110792.1:)		 c.1440G>A
Alternate Protein name
(NP_001104262)		 p.(=)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153295875C>T
Mutation type Silent
Domain C-term
Pathogenicity Silent polymorphism
Evidence of Pathogenicity
Detection Not known
Extent Exons 2-4 (at least)
Source of DNA Blood or skin
Carrier NC
Carrier result
Other mutations N
X-inactivation results
X-inactivation relatives
Gender Male
Sporadic/Familial Not known
Phenotype-class Not Known
Reference :Cardiff, UK::

Matching entries in the proband database


No: Systematic Name Protein name Gender Carrier result Phenotype Proband id Reference
1 c.1404G>A p.Arg468Arg Male Not Known 2142 :Cardiff, UK::