U.S. flag

An official website of the United States government

NM_000136.3(FANCC):c.349G>A (p.Val117Ile) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 27, 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:
RCV000482048.3

Allele description [Variation Report for NM_000136.3(FANCC):c.349G>A (p.Val117Ile)]

NM_000136.3(FANCC):c.349G>A (p.Val117Ile)

Gene:
FANCC:FA complementation group C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q22.32
Genomic location:
Preferred name:
NM_000136.3(FANCC):c.349G>A (p.Val117Ile)
HGVS:
  • NC_000009.12:g.95172144C>T
  • NG_011707.1:g.150566G>A
  • NM_000136.3:c.349G>AMANE SELECT
  • NM_001243743.2:c.349G>A
  • NM_001243744.2:c.349G>A
  • NP_000127.2:p.Val117Ile
  • NP_001230672.1:p.Val117Ile
  • NP_001230673.1:p.Val117Ile
  • LRG_497t1:c.349G>A
  • LRG_497:g.150566G>A
  • NC_000009.11:g.97934426C>T
  • NM_000136.2:c.349G>A
Protein change:
V117I
Links:
dbSNP: rs781167993
NCBI 1000 Genomes Browser:
rs781167993
Molecular consequence:
  • NM_000136.3:c.349G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001243743.2:c.349G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001243744.2:c.349G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000571121GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Feb 27, 2024) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV000571121.6

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 35264596, Gordon2000[Book])

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

Last Updated: Oct 8, 2024