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NM_002878.4(RAD51D):c.355T>C (p.Cys119Arg) AND Hereditary breast ovarian cancer syndrome

Germline classification:
Likely benign (1 submission)
Last evaluated:
Apr 9, 2024
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000709444.5

Allele description [Variation Report for NM_002878.4(RAD51D):c.355T>C (p.Cys119Arg)]

NM_002878.4(RAD51D):c.355T>C (p.Cys119Arg)

Genes:
RAD51D:RAD51 paralog D [Gene - OMIM - HGNC]
RAD51L3-RFFL:RAD51L3-RFFL readthrough [Gene]
Variant type:
single nucleotide variant
Cytogenetic location:
17q12
Genomic location:
Preferred name:
NM_002878.4(RAD51D):c.355T>C (p.Cys119Arg)
Other names:
p.C119R:TGT>CGT
HGVS:
  • NC_000017.11:g.35107113A>G
  • NG_031858.1:g.17757T>C
  • NM_001142571.2:c.415T>C
  • NM_002878.4:c.355T>CMANE SELECT
  • NM_133629.3:c.145-632T>C
  • NP_001136043.1:p.Cys139Arg
  • NP_002869.3:p.Cys119Arg
  • NP_002869.3:p.Cys119Arg
  • LRG_516t1:c.355T>C
  • LRG_516:g.17757T>C
  • LRG_516p1:p.Cys119Arg
  • NC_000017.10:g.33434132A>G
  • NM_002878.3:c.355T>C
  • NR_037711.2:n.381T>C
  • p.C119R
Protein change:
C119R
Links:
dbSNP: rs201313861
NCBI 1000 Genomes Browser:
rs201313861
Molecular consequence:
  • NM_133629.3:c.145-632T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001142571.2:c.415T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002878.4:c.355T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NR_037711.2:n.381T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Hereditary breast ovarian cancer syndrome
Synonyms:
Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000839188Mendelics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely benign
(Apr 9, 2024) 		unknownclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Mendelics, SCV000839188.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024