NM_058216.3(RAD51C):c.237T>A (p.Ser79=) AND Fanconi anemia complementation group O

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jul 12, 2023
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:: RCV003506812.2

Allele description [Variation Report for NM_058216.3(RAD51C):c.237T>A (p.Ser79=)]

NM_058216.3(RAD51C):c.237T>A (p.Ser79=)

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.237T>A (p.Ser79=)

HGVS:

NC_000017.11:g.58695022T>A
NG_023199.1:g.7421T>A
NG_047169.1:g.2058A>T
NM_002876.4:c.237T>A
NM_058216.3:c.237T>AMANE SELECT
NM_058217.1:c.237T>A
NP_002867.1:p.Ser79=
NP_478123.1:p.Ser79=
NP_478123.1:p.Ser79=
NP_478124.1:p.Ser79=
LRG_314t1:c.237T>A
LRG_314:g.7421T>A
LRG_314p1:p.Ser79=
NC_000017.10:g.56772383T>A
NM_058216.1:c.237T>A
NR_103872.2:n.279T>A
NR_103873.1:n.205T>A

Molecular consequence:

NR_103872.2:n.279T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_103873.1:n.205T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_002876.4:c.237T>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_058216.3:c.237T>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_058217.1:c.237T>A - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Fanconi anemia complementation group O
Identifiers:: MONDO: MONDO:0013248; MedGen: C3150653; Orphanet: 84; OMIM: 613390

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004304650	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Jul 12, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004304650

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Jul 12, 2023)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV004304650.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine