U.S. flag

An official website of the United States government

NM_005591.4(MRE11):c.605G>A (p.Arg202Lys) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 20, 2017
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:
RCV000569107.3

Allele description [Variation Report for NM_005591.4(MRE11):c.605G>A (p.Arg202Lys)]

NM_005591.4(MRE11):c.605G>A (p.Arg202Lys)

Gene:
MRE11:MRE11 homolog, double strand break repair nuclease [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q21
Genomic location:
Preferred name:
NM_005591.4(MRE11):c.605G>A (p.Arg202Lys)
HGVS:
  • NC_000011.10:g.94476343C>T
  • NG_007261.1:g.22532G>A
  • NM_001330347.2:c.605G>A
  • NM_005590.4:c.605G>A
  • NM_005591.4:c.605G>AMANE SELECT
  • NP_001317276.1:p.Arg202Lys
  • NP_005581.2:p.Arg202Lys
  • NP_005582.1:p.Arg202Lys
  • NP_005582.1:p.Arg202Lys
  • LRG_85t1:c.605G>A
  • LRG_85:g.22532G>A
  • LRG_85p1:p.Arg202Lys
  • NC_000011.9:g.94209509C>T
  • NM_005591.3:c.605G>A
Protein change:
R202K
Links:
dbSNP: rs1555014514
NCBI 1000 Genomes Browser:
rs1555014514
Molecular consequence:
  • NM_001330347.2:c.605G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_005590.4:c.605G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_005591.4:c.605G>A - 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

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
SCV000662203Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Jul 20, 2017) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV000662203.5

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

Description

The p.R202K variant (also known as c.605G>A), located in coding exon 6 of the MRE11A gene, results from a G to A substitution at nucleotide position 605. The arginine at codon 202 is replaced by lysine, an amino acid with highly similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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

Last Updated: May 1, 2024