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NM_001370259.2(MEN1):c.1526G>T (p.Gly509Val) AND Multiple endocrine neoplasia, type 1

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 24, 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:
RCV000632099.7

Allele description [Variation Report for NM_001370259.2(MEN1):c.1526G>T (p.Gly509Val)]

NM_001370259.2(MEN1):c.1526G>T (p.Gly509Val)

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.1526G>T (p.Gly509Val)
HGVS:
  • NC_000011.10:g.64804641C>A
  • NG_008929.1:g.11654G>T
  • NG_033040.1:g.3601G>T
  • NM_000244.4:c.1541G>T
  • NM_001370251.2:c.1652G>T
  • NM_001370259.2:c.1526G>TMANE SELECT
  • NM_001370260.2:c.1526G>T
  • NM_001370261.2:c.1526G>T
  • NM_001370262.2:c.1421G>T
  • NM_001370263.2:c.1421G>T
  • NM_130799.3:c.1526G>T
  • NM_130800.3:c.1541G>T
  • NM_130801.3:c.1541G>T
  • NM_130802.3:c.1541G>T
  • NM_130803.3:c.1541G>T
  • NM_130804.3:c.1541G>T
  • NP_000235.3:p.Gly514Val
  • NP_001357180.2:p.Gly551Val
  • NP_001357188.2:p.Gly509Val
  • NP_001357189.2:p.Gly509Val
  • NP_001357190.2:p.Gly509Val
  • NP_001357191.2:p.Gly474Val
  • NP_001357192.2:p.Gly474Val
  • NP_570711.1:p.Gly509Val
  • NP_570711.2:p.Gly509Val
  • NP_570712.2:p.Gly514Val
  • NP_570713.2:p.Gly514Val
  • NP_570714.2:p.Gly514Val
  • NP_570715.2:p.Gly514Val
  • NP_570716.2:p.Gly514Val
  • LRG_509t2:c.1526G>T
  • LRG_509:g.11654G>T
  • LRG_509p2:p.Gly509Val
  • NC_000011.9:g.64572113C>A
  • NM_130799.2:c.1526G>T
Protein change:
G474V
Links:
dbSNP: rs769355346
NCBI 1000 Genomes Browser:
rs769355346
Molecular consequence:
  • NM_000244.4:c.1541G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370251.2:c.1652G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370259.2:c.1526G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370260.2:c.1526G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370261.2:c.1526G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370262.2:c.1421G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370263.2:c.1421G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130799.3:c.1526G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130800.3:c.1541G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130801.3:c.1541G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130802.3:c.1541G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130803.3:c.1541G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130804.3:c.1541G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Multiple endocrine neoplasia, type 1 (MEN1)
Synonyms:
MEA I; MEN I; Endocrine adenomatosis multiple; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0007540; MeSH: D018761; MedGen: C0025267; Orphanet: 652; OMIM: 131100

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000753203Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Nov 24, 2017) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000753203.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with MEN1-related disease. This variant is not present in population databases (ExAC no frequency). This sequence change replaces glycine with valine at codon 509 of the MEN1 protein (p.Gly509Val). The glycine residue is moderately conserved and there is a moderate physicochemical difference between glycine and valine.

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

Last Updated: Sep 29, 2024