Project HERA
RAD51D variants
Every RAD51D variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
RAD51D variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
RAD51D
NM_002878.4:c.694C>T
NP_002869.3:p.(R232*)
Likely Pathogenic
View →
RAD51D
NM_002878.4:c.715C>T
NP_002869.3:p.(R239W)
Likely Benign
View →
RAD51D
NM_002878.4:c.270_271dup
NP_002869.3:p.(K91Ifs*13)
Pathogenic
View →
RAD51D
NM_002878.4:c.829C>G
NP_002869.3:p.(L277V)
VUS
View →
RAD51D
NM_002878.3:c.26G>C
NP_002869.3:p.(C9S)
Likely Benign
View →
RAD51D
NM_002878.3:c.26G>T
NP_002869.3:p.(C9F)
VUS
View →
RAD51D
NM_002878.3:c.422T>C
NP_002869.3:p.(L141P)
VUS
View →
RAD51D
NM_002878.3:c.641C>T
NP_002869.3:p.(P214L)
VUS
View →
RAD51D
NM_002878.4:c.198G>T
NP_002869.3:p.(V66=)
Likely Benign
View →
RAD51D
NM_002878.4:c.446T>A
NP_002869.3:p.(L149Q)
VUS
View →