NM_002382.5(MAX):c.406G>C (p.Gly136Arg) AND Hereditary cancer-predisposing syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 4, 2024
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:: RCV002324495.3

Allele description [Variation Report for NM_002382.5(MAX):c.406G>C (p.Gly136Arg)]

NM_002382.5(MAX):c.406G>C (p.Gly136Arg)

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.406G>C (p.Gly136Arg)

HGVS:

NC_000014.9:g.65076553C>G
NG_029830.1:g.30957G>C
NM_001271069.2:c.144+17155G>C
NM_001320415.2:c.217G>C
NM_001407094.1:c.406G>C
NM_001407095.1:c.379G>C
NM_001407096.1:c.*179G>C
NM_001407097.1:c.*195G>C
NM_001407098.1:c.298G>C
NM_001407099.1:c.*179G>C
NM_001407100.1:c.*195G>C
NM_001407101.1:c.*195G>C
NM_001407102.1:c.*179G>C
NM_001407103.1:c.*195G>C
NM_001407104.1:c.*179G>C
NM_001407105.1:c.217G>C
NM_001407106.1:c.217G>C
NM_001407107.1:c.217G>C
NM_001407108.1:c.*179G>C
NM_001407109.1:c.*195G>C
NM_001407110.1:c.*195G>C
NM_001407111.1:c.205G>C
NM_001407112.1:c.205G>C
NM_002382.5:c.406G>CMANE SELECT
NM_145112.3:c.379G>C
NM_145113.3:c.*195G>C
NM_197957.4:c.171+17155G>C
NP_001307344.1:p.Gly73Arg
NP_001394023.1:p.Gly136Arg
NP_001394024.1:p.Gly127Arg
NP_001394027.1:p.Gly100Arg
NP_001394034.1:p.Gly73Arg
NP_001394035.1:p.Gly73Arg
NP_001394036.1:p.Gly73Arg
NP_001394040.1:p.Gly69Arg
NP_001394041.1:p.Gly69Arg
NP_002373.3:p.Gly136Arg
NP_002373.3:p.Gly136Arg
NP_660087.1:p.Gly127Arg
LRG_530t1:c.406G>C
LRG_530:g.30957G>C
LRG_530p1:p.Gly136Arg
NC_000014.8:g.65543271C>G
NM_002382.3:c.406G>C
NR_073137.1:n.530G>C
NR_073137.2:n.530G>C
NR_176275.1:n.649G>C
NR_176278.1:n.379G>C
NR_176279.1:n.583G>C
NR_176280.1:n.548G>C
NR_176281.1:n.730G>C
NR_176282.1:n.453G>C

Protein change:

G100R

Links:

dbSNP: rs140490467

NCBI 1000 Genomes Browser:

rs140490467

Molecular consequence:

NM_145113.3:c.*195G>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001271069.2:c.144+17155G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_197957.4:c.171+17155G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001320415.2:c.217G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407094.1:c.406G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407095.1:c.379G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407098.1:c.298G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407105.1:c.217G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407106.1:c.217G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407107.1:c.217G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407111.1:c.205G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407112.1:c.205G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_002382.5:c.406G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_145112.3:c.379G>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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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002631382	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (May 4, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002631382

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(May 4, 2024)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV002631382.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The p.G136R variant (also known as c.406G>C), located in coding exon 5 of the MAX gene, results from a G to C substitution at nucleotide position 406. The glycine at codon 136 is replaced by arginine, an amino acid with dissimilar 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.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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