Proband information


Proband id 1662
Systematic Name
(NM_004992.3:)
c.1271_1416del146
Protein name
(NP_004983)
p.Leu424fs
Alternate systematic Name
(NM_001110792.1:)
c.1307_1452del146
Alternate Protein name
(NP_001104262)
p.(Leu436Argfs*14)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)
g.153295863_153296008del146
Mutation type Frameshift insertion or deletion
Domain C-term
Pathogenicity Mutation associated with disease
Evidence of Pathogenicity
Detection direct
Extent Exons 2-4
Source of DNA blood
Carrier NC
Carrier result
Other mutations N
X-inactivation results
X-inactivation relatives
Gender Female
Sporadic/Familial Not known
Phenotype-class Not Known
Reference :Friez, Michael::

Matching entries in the proband database


No: Systematic Name Protein name Gender Carrier result Phenotype Proband id Reference
1 c.1271_1416del146 p.Leu424fs Female Not Known 1662 :Friez, Michael::