NM_001048174.2(MUTYH):c.262C>G (p.Arg88Gly) AND Familial adenomatous polyposis 2

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 24, 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:: RCV001061774.9

Allele description [Variation Report for NM_001048174.2(MUTYH):c.262C>G (p.Arg88Gly)]

NM_001048174.2(MUTYH):c.262C>G (p.Arg88Gly)

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.262C>G (p.Arg88Gly)

HGVS:

NC_000001.11:g.45333415G>C
NG_008189.1:g.12056C>G
NM_001048171.2:c.262C>G
NM_001048172.2:c.265C>G
NM_001048173.2:c.262C>G
NM_001048174.2:c.262C>GMANE SELECT
NM_001128425.2:c.346C>G
NM_001293190.2:c.307C>G
NM_001293191.2:c.295C>G
NM_001293192.2:c.-15C>G
NM_001293195.2:c.262C>G
NM_001293196.2:c.-15C>G
NM_001350650.2:c.-10C>G
NM_001350651.2:c.-10C>G
NM_012222.3:c.337C>G
NP_001041636.2:p.Arg88Gly
NP_001041637.1:p.Arg89Gly
NP_001041638.1:p.Arg88Gly
NP_001041639.1:p.Arg88Gly
NP_001121897.1:p.Arg116Gly
NP_001280119.1:p.Arg103Gly
NP_001280120.1:p.Arg99Gly
NP_001280124.1:p.Arg88Gly
NP_036354.1:p.Arg113Gly
LRG_220t1:c.346C>G
LRG_220:g.12056C>G
NC_000001.10:g.45799087G>C
NM_001128425.1:c.346C>G
NR_146882.2:n.490C>G
NR_146883.2:n.413C>G

Protein change:

R103G

Links:

dbSNP: rs373766973

NCBI 1000 Genomes Browser:

rs373766973

Molecular consequence:

NM_001293192.2:c.-15C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001293196.2:c.-15C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001350650.2:c.-10C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001350651.2:c.-10C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001048171.2:c.262C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001048172.2:c.265C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001048173.2:c.262C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001048174.2:c.262C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001128425.2:c.346C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001293190.2:c.307C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001293191.2:c.295C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001293195.2:c.262C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_012222.3:c.337C>G - missense variant - [Sequence Ontology: SO:0001583]
NR_146882.2:n.490C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_146883.2:n.413C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Familial adenomatous polyposis 2
Synonyms:: COLORECTAL ADENOMATOUS POLYPOSIS, AUTOSOMAL RECESSIVE; ADENOMAS, MULTIPLE COLORECTAL, AUTOSOMAL RECESSIVE; MYH-associated polyposis; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0012041; MedGen: C3272841; Orphanet: 220460; OMIM: 608456

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001226530	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Nov 24, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001226530

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Nov 24, 2023)

germline

clinical testing

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

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

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, SCV001226530.5

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

Description

This sequence change replaces arginine, which is basic and polar, with glycine, which is neutral and non-polar, at codon 116 of the MUTYH protein (p.Arg116Gly). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with MUTYH-related conditions. ClinVar contains an entry for this variant (Variation ID: 823807). An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant¬†is likely to be tolerated. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. 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.

#	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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