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NM_000136.3(FANCC):c.1326T>C (p.Thr442=) AND Hereditary cancer-predisposing syndrome

Germline classification:
Likely benign (1 submission)
Last evaluated:
Nov 27, 2022
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:
RCV003171539.2

Allele description [Variation Report for NM_000136.3(FANCC):c.1326T>C (p.Thr442=)]

NM_000136.3(FANCC):c.1326T>C (p.Thr442=)

Genes:
FANCC:FA complementation group C [Gene - OMIM - HGNC]
AOPEP:aminopeptidase O (putative) [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q22.32
Genomic location:
Preferred name:
NM_000136.3(FANCC):c.1326T>C (p.Thr442=)
HGVS:
  • NC_000009.12:g.95111466A>G
  • NG_011707.1:g.211244T>C
  • NG_027833.2:g.389769A>G
  • NM_000136.3:c.1326T>CMANE SELECT
  • NM_001243743.2:c.1326T>C
  • NM_001243744.2:c.1326T>C
  • NP_000127.2:p.Thr442=
  • NP_000127.2:p.Thr442=
  • NP_001230672.1:p.Thr442=
  • NP_001230673.1:p.Thr442=
  • LRG_497t1:c.1326T>C
  • LRG_497:g.211244T>C
  • LRG_497p1:p.Thr442=
  • NC_000009.11:g.97873748A>G
  • NM_000136.2:c.1326T>C
Molecular consequence:
  • NM_000136.3:c.1326T>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001243743.2:c.1326T>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001243744.2:c.1326T>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
SCV003859382Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Nov 27, 2022) 		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, SCV003859382.2

#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