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NM_002485.5(NBN):c.845T>C (p.Ile282Thr) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Sep 13, 2014
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:
RCV000165493.3

Allele description [Variation Report for NM_002485.5(NBN):c.845T>C (p.Ile282Thr)]

NM_002485.5(NBN):c.845T>C (p.Ile282Thr)

Gene:
NBN:nibrin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8q21.3
Genomic location:
Preferred name:
NM_002485.5(NBN):c.845T>C (p.Ile282Thr)
HGVS:
  • NC_000008.11:g.89970415A>G
  • NG_008860.1:g.19257T>C
  • NM_001024688.3:c.599T>C
  • NM_002485.5:c.845T>CMANE SELECT
  • NP_001019859.1:p.Ile200Thr
  • NP_002476.2:p.Ile282Thr
  • NP_002476.2:p.Ile282Thr
  • LRG_158t1:c.845T>C
  • LRG_158:g.19257T>C
  • LRG_158p1:p.Ile282Thr
  • NC_000008.10:g.90982643A>G
  • NM_002485.4:c.845T>C
  • p.I282T
Protein change:
I200T
Links:
dbSNP: rs786202604
NCBI 1000 Genomes Browser:
rs786202604
Molecular consequence:
  • NM_001024688.3:c.599T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002485.5:c.845T>C - missense variant - [Sequence Ontology: SO:0001583]

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
SCV000216224Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Sep 13, 2014) 		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, SCV000216224.7

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

Description

The p.I282T variant (also known as c.845T>C), located in coding exon 7 of the NBN gene, results from a T to C substitution at nucleotide position 845. The isoleucine at codon 282 is replaced by threonine, an amino acid with similar properties. This variant was not reported in population based cohorts in the following databases: Database of Single Nucleotide Polymorphisms (dbSNP), NHLBI Exome Sequencing Project (ESP), and 1000 Genomes Project. In the ESP, this variant was not observed in 6503 samples (13006 alleles) with coverage at this position. To date, this alteration has been detected with an allele frequency of approximately 0.005% (greater than 22,000 alleles tested) in our clinical cohort (includes this individual). Based on protein sequence alignment, this amino acid position is poorly conserved in lower vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of p.I282T remains unclear.

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

Last Updated: May 1, 2024