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  3. RAD51D
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Multiple Tumours

Gene: RAD51D

Green List (high evidence)
RAD51D (RAD51 paralog D)
EnsemblGeneIds (GRCh38): ENSG00000185379
EnsemblGeneIds (GRCh37): ENSG00000185379
OMIM: 602954, Gene2Phenotype
RAD51D is in 6 panels

1 review

Ellen McDonagh (Genomics England Curator)

Information from TruSight panel: Pathogenic Mutations are Inactivating.
Created: 5 Feb 2016, 11:47 a.m.
Created: 5 Feb 2016, 11:47 a.m.

Panel version: 0.2

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • TruSight Cancer Panel (Illumina)
Phenotypes
  • Ovarian cancer
  • Familial breast cancer
OMIM
602954
Clinvar variants
Variants in RAD51D
Penetrance
Complete
Panels with this gene

History Filter Activity

9 Mar 2016, Gel status: 4

Set Mode of Inheritance, Added New Source

Ellen McDonagh (Genomics England Curator)

RAD51D was added to Multiple Tumourspanel. Source: Expert Review Green Model of inheritance for gene RAD51D was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

5 Feb 2016, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

RAD51D was created by ellenmcdonagh

5 Feb 2016, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

RAD51D was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)