U.S. flag

An official website of the United States government

NM_001048174.2(MUTYH):c.1226G>T (p.Arg409Leu) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Mar 16, 2023
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV000131605.8

Allele description [Variation Report for NM_001048174.2(MUTYH):c.1226G>T (p.Arg409Leu)]

NM_001048174.2(MUTYH):c.1226G>T (p.Arg409Leu)

Gene:
MUTYH:mutY DNA glycosylase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p34.1
Genomic location:
Preferred name:
NM_001048174.2(MUTYH):c.1226G>T (p.Arg409Leu)
HGVS:
  • NC_000001.11:g.45331433C>A
  • NG_008189.1:g.14038G>T
  • NM_001048171.2:c.1226G>T
  • NM_001048172.2:c.1229G>T
  • NM_001048173.2:c.1226G>T
  • NM_001048174.2:c.1226G>TMANE SELECT
  • NM_001128425.2:c.1310G>T
  • NM_001293190.2:c.1271G>T
  • NM_001293191.2:c.1259G>T
  • NM_001293192.2:c.950G>T
  • NM_001293195.2:c.1226G>T
  • NM_001293196.2:c.950G>T
  • NM_001350650.2:c.881G>T
  • NM_001350651.2:c.881G>T
  • NM_012222.3:c.1301G>T
  • NP_001041636.2:p.Arg409Leu
  • NP_001041637.1:p.Arg410Leu
  • NP_001041638.1:p.Arg409Leu
  • NP_001041639.1:p.Arg409Leu
  • NP_001121897.1:p.Arg437Leu
  • NP_001121897.1:p.Arg437Leu
  • NP_001280119.1:p.Arg424Leu
  • NP_001280120.1:p.Arg420Leu
  • NP_001280121.1:p.Arg317Leu
  • NP_001280124.1:p.Arg409Leu
  • NP_001280125.1:p.Arg317Leu
  • NP_001337579.1:p.Arg294Leu
  • NP_001337580.1:p.Arg294Leu
  • NP_036354.1:p.Arg434Leu
  • LRG_220t1:c.1310G>T
  • LRG_220:g.14038G>T
  • LRG_220p1:p.Arg437Leu
  • NC_000001.10:g.45797105C>A
  • NM_001128425.1:c.1310G>T
  • NR_146882.2:n.1454G>T
  • NR_146883.2:n.1303G>T
  • p.R437L
Protein change:
R294L
Links:
dbSNP: rs587782120
NCBI 1000 Genomes Browser:
rs587782120
Molecular consequence:
  • NM_001048171.2:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001048172.2:c.1229G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001048173.2:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001048174.2:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001128425.2:c.1310G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293190.2:c.1271G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293191.2:c.1259G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293192.2:c.950G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293195.2:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293196.2:c.950G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001350650.2:c.881G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001350651.2:c.881G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_012222.3:c.1301G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_146882.2:n.1454G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_146883.2:n.1303G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

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
SCV000186621Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Sep 21, 2022) 		germlineclinical testing

Citation Link,

SCV001352098Color Diagnostics, LLC DBA Color Health
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Mar 16, 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

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Ambry Genetics, SCV000186621.8

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

Description

The p.R437L variant (also known as c.1310G>T), located in coding exon 13 of the MUTYH gene, results from a G to T substitution at nucleotide position 1310. The arginine at codon 437 is replaced by leucine, an amino acid with dissimilar properties. This amino acid position is not well 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

From Color Diagnostics, LLC DBA Color Health, SCV001352098.2

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

Description

This missense variant replaces arginine with leucine at codon 437 of the MUTYH protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with MUTYH-related disorders in the literature. This variant has been identified in 2/251368 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is 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