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NM_001370259.2(MEN1):c.1379G>T (p.Arg460Leu) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 8, 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:
RCV002381115.2

Allele description [Variation Report for NM_001370259.2(MEN1):c.1379G>T (p.Arg460Leu)]

NM_001370259.2(MEN1):c.1379G>T (p.Arg460Leu)

Gene:
MEN1:menin 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q13.1
Genomic location:
Preferred name:
NM_001370259.2(MEN1):c.1379G>T (p.Arg460Leu)
HGVS:
  • NC_000011.10:g.64804788C>A
  • NG_008929.1:g.11507G>T
  • NG_033040.2:g.3426G>T
  • NM_000244.4:c.1394G>T
  • NM_001370251.2:c.1505G>T
  • NM_001370259.2:c.1379G>TMANE SELECT
  • NM_001370260.2:c.1379G>T
  • NM_001370261.2:c.1379G>T
  • NM_001370262.2:c.1274G>T
  • NM_001370263.2:c.1274G>T
  • NM_001407142.1:c.1505G>T
  • NM_001407143.1:c.1505G>T
  • NM_001407144.1:c.1505G>T
  • NM_001407145.1:c.1394G>T
  • NM_001407146.1:c.1379G>T
  • NM_001407147.1:c.1379G>T
  • NM_001407148.1:c.1274G>T
  • NM_001407149.1:c.1274G>T
  • NM_001407150.1:c.1520G>T
  • NM_001407151.1:c.1400G>T
  • NM_001407152.1:c.1214G>T
  • NM_130799.3:c.1379G>T
  • NM_130800.3:c.1394G>T
  • NM_130801.3:c.1394G>T
  • NM_130802.3:c.1394G>T
  • NM_130803.3:c.1394G>T
  • NM_130804.3:c.1394G>T
  • NP_000235.2:p.Arg465Leu
  • NP_000235.3:p.Arg465Leu
  • NP_001357180.2:p.Arg502Leu
  • NP_001357188.2:p.Arg460Leu
  • NP_001357189.2:p.Arg460Leu
  • NP_001357190.2:p.Arg460Leu
  • NP_001357191.2:p.Arg425Leu
  • NP_001357192.2:p.Arg425Leu
  • NP_001394071.1:p.Arg502Leu
  • NP_001394072.1:p.Arg502Leu
  • NP_001394073.1:p.Arg502Leu
  • NP_001394074.1:p.Arg465Leu
  • NP_001394075.1:p.Arg460Leu
  • NP_001394076.1:p.Arg460Leu
  • NP_001394077.1:p.Arg425Leu
  • NP_001394078.1:p.Arg425Leu
  • NP_001394079.1:p.Arg507Leu
  • NP_001394080.1:p.Arg467Leu
  • NP_001394081.1:p.Arg405Leu
  • NP_570711.1:p.Arg460Leu
  • NP_570711.2:p.Arg460Leu
  • NP_570712.2:p.Arg465Leu
  • NP_570713.2:p.Arg465Leu
  • NP_570714.2:p.Arg465Leu
  • NP_570715.2:p.Arg465Leu
  • NP_570716.2:p.Arg465Leu
  • LRG_509t1:c.1394G>T
  • LRG_509t2:c.1379G>T
  • LRG_509:g.11507G>T
  • LRG_509p1:p.Arg465Leu
  • LRG_509p2:p.Arg460Leu
  • NC_000011.9:g.64572260C>A
  • NG_033040.1:g.3454G>T
  • NM_000244.3:c.1394G>T
  • NM_130799.2:c.1379G>T
  • NR_176284.1:n.1577G>T
  • NR_176285.1:n.1589G>T
  • NR_176286.1:n.1592G>T
  • NR_176287.1:n.1850G>T
Protein change:
R405L
Molecular consequence:
  • NM_000244.4:c.1394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370251.2:c.1505G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370259.2:c.1379G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370260.2:c.1379G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370261.2:c.1379G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370262.2:c.1274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370263.2:c.1274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407142.1:c.1505G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407143.1:c.1505G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407144.1:c.1505G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407145.1:c.1394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407146.1:c.1379G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407147.1:c.1379G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407148.1:c.1274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407149.1:c.1274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407150.1:c.1520G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407151.1:c.1400G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407152.1:c.1214G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130799.3:c.1379G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130800.3:c.1394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130801.3:c.1394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130802.3:c.1394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130803.3:c.1394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130804.3:c.1394G>T - 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
SCV002696711Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Mar 8, 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, SCV002696711.2

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

Description

The p.R460L variant (also known as c.1379G>T), located in coding exon 9 of the MEN1 gene, results from a G to T substitution at nucleotide position 1379. The arginine at codon 460 is replaced by leucine, an amino acid with dissimilar properties. This amino acid position is conserved. 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