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NM_058216.3(RAD51C):c.54G>C (p.Pro18=) AND Hereditary cancer-predisposing syndrome

Germline classification:
Likely benign (1 submission)
Last evaluated:
May 8, 2021
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:
RCV002351649.2

Allele description [Variation Report for NM_058216.3(RAD51C):c.54G>C (p.Pro18=)]

NM_058216.3(RAD51C):c.54G>C (p.Pro18=)

Gene:
RAD51C:RAD51 paralog C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q22
Genomic location:
Preferred name:
NM_058216.3(RAD51C):c.54G>C (p.Pro18=)
HGVS:
  • NC_000017.11:g.58692697G>C
  • NG_023199.1:g.5096G>C
  • NG_047169.1:g.4383C>G
  • NM_002876.4:c.54G>C
  • NM_058216.3:c.54G>CMANE SELECT
  • NM_058217.1:c.54G>C
  • NP_002867.1:p.Pro18=
  • NP_478123.1:p.Pro18=
  • NP_478123.1:p.Pro18=
  • NP_478124.1:p.Pro18=
  • LRG_314t1:c.54G>C
  • LRG_314:g.5096G>C
  • LRG_314p1:p.Pro18=
  • NC_000017.10:g.56770058G>C
  • NM_058216.1:c.54G>C
  • NR_103872.2:n.96G>C
Molecular consequence:
  • NR_103872.2:n.96G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_002876.4:c.54G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_058216.3:c.54G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_058217.1:c.54G>C - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002648643Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(May 8, 2021) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV002648643.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: May 1, 2024