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NM_002382.5(MAX):c.331C>G (p.Leu111Val) AND Hereditary pheochromocytoma-paraganglioma

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 11, 2023
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:
RCV000639345.11

Allele description [Variation Report for NM_002382.5(MAX):c.331C>G (p.Leu111Val)]

NM_002382.5(MAX):c.331C>G (p.Leu111Val)

Gene:
MAX:MYC associated factor X [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
14q23.3
Genomic location:
Preferred name:
NM_002382.5(MAX):c.331C>G (p.Leu111Val)
HGVS:
  • NC_000014.9:g.65076628G>C
  • NG_029830.1:g.30882C>G
  • NM_001271069.2:c.144+17080C>G
  • NM_001320415.2:c.142C>G
  • NM_001407094.1:c.331C>G
  • NM_001407095.1:c.304C>G
  • NM_001407096.1:c.*104C>G
  • NM_001407097.1:c.*120C>G
  • NM_001407098.1:c.223C>G
  • NM_001407099.1:c.*104C>G
  • NM_001407100.1:c.*120C>G
  • NM_001407101.1:c.*120C>G
  • NM_001407102.1:c.*104C>G
  • NM_001407103.1:c.*120C>G
  • NM_001407104.1:c.*104C>G
  • NM_001407105.1:c.142C>G
  • NM_001407106.1:c.142C>G
  • NM_001407107.1:c.142C>G
  • NM_001407108.1:c.*104C>G
  • NM_001407109.1:c.*120C>G
  • NM_001407110.1:c.*120C>G
  • NM_001407111.1:c.130C>G
  • NM_001407112.1:c.130C>G
  • NM_002382.5:c.331C>GMANE SELECT
  • NM_145112.3:c.304C>G
  • NM_145113.3:c.*120C>G
  • NM_197957.4:c.171+17080C>G
  • NP_001307344.1:p.Leu48Val
  • NP_001394023.1:p.Leu111Val
  • NP_001394024.1:p.Leu102Val
  • NP_001394027.1:p.Leu75Val
  • NP_001394034.1:p.Leu48Val
  • NP_001394035.1:p.Leu48Val
  • NP_001394036.1:p.Leu48Val
  • NP_001394040.1:p.Leu44Val
  • NP_001394041.1:p.Leu44Val
  • NP_002373.3:p.Leu111Val
  • NP_002373.3:p.Leu111Val
  • NP_660087.1:p.Leu102Val
  • LRG_530t1:c.331C>G
  • LRG_530:g.30882C>G
  • LRG_530p1:p.Leu111Val
  • NC_000014.8:g.65543346G>C
  • NM_002382.3:c.331C>G
  • NM_002382.4:c.331C>G
  • NR_073137.1:n.455C>G
  • NR_073137.2:n.455C>G
  • NR_176275.1:n.574C>G
  • NR_176278.1:n.304C>G
  • NR_176279.1:n.508C>G
  • NR_176280.1:n.473C>G
  • NR_176281.1:n.655C>G
  • NR_176282.1:n.378C>G
Protein change:
L102V
Links:
dbSNP: rs748675729
NCBI 1000 Genomes Browser:
rs748675729
Molecular consequence:
  • NM_145113.3:c.*120C>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001271069.2:c.144+17080C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_197957.4:c.171+17080C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001320415.2:c.142C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407094.1:c.331C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407095.1:c.304C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407098.1:c.223C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407105.1:c.142C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407106.1:c.142C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407107.1:c.142C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407111.1:c.130C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407112.1:c.130C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002382.5:c.331C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_145112.3:c.304C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hereditary pheochromocytoma-paraganglioma
Synonyms:
Hereditary Paraganglioma-Pheochromocytoma Syndromes; Hereditary Paragangliomas and Pheochromocytomas
Identifiers:
MONDO: MONDO:0017366; MedGen: C1708353

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000760917Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Oct 11, 2023) 		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, SCV000760917.7

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

Description

This sequence change replaces leucine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 111 of the MAX protein (p.Leu111Val). This variant is present in population databases (rs748675729, gnomAD 0.002%). This variant has not been reported in the literature in individuals affected with MAX-related conditions. ClinVar contains an entry for this variant (Variation ID: 485703). Advanced modeling performed at Invitae incorporating data from internal and/or published experimental studies (Invitae) indicates that this missense variant is not expected to disrupt MAX function. 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.

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

Last Updated: Sep 29, 2024