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NM_001048174.2(MUTYH):c.1435-84_1512del AND Familial adenomatous polyposis 2

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 4, 2022
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:
RCV003000223.2

Allele description [Variation Report for NM_001048174.2(MUTYH):c.1435-84_1512del]

NM_001048174.2(MUTYH):c.1435-84_1512del

Gene:
MUTYH:mutY DNA glycosylase [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
1p34.1
Genomic location:
Preferred name:
NM_001048174.2(MUTYH):c.1435-84_1512del
HGVS:
  • NC_000001.11:g.45329362_45329523del
  • NG_008189.1:g.15950_16111del
  • NG_090898.1:g.8_169del
  • NM_001048171.2:c.1435-84_1512del
  • NM_001048172.2:c.1438-84_1515del
  • NM_001048173.2:c.1435-84_1512del
  • NM_001048174.2:c.1435-84_1512delMANE SELECT
  • NM_001128425.2:c.1519-84_1596del
  • NM_001293190.2:c.1480-84_1557del
  • NM_001293191.2:c.1468-84_1545del
  • NM_001293192.2:c.1159-84_1236del
  • NM_001293195.2:c.1435-84_1512del
  • NM_001293196.2:c.1159-84_1236del
  • NM_001350650.2:c.1090-84_1167del
  • NM_001350651.2:c.1090-84_1167del
  • NM_012222.3:c.1510-84_1587del
  • LRG_220:g.15950_16111del
  • NC_000001.10:g.45795032_45795193del
  • NC_000001.10:g.45795034_45795195del
Molecular consequence:
  • NM_001048171.2:c.1435-84_1512del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001048172.2:c.1438-84_1515del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001048173.2:c.1435-84_1512del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001048174.2:c.1435-84_1512del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001128425.2:c.1519-84_1596del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001293190.2:c.1480-84_1557del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001293191.2:c.1468-84_1545del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001293192.2:c.1159-84_1236del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001293195.2:c.1435-84_1512del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001293196.2:c.1159-84_1236del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001350650.2:c.1090-84_1167del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001350651.2:c.1090-84_1167del - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_012222.3:c.1510-84_1587del - splice acceptor variant - [Sequence Ontology: SO:0001574]

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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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003304699Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Oct 4, 2022) 		germlineclinical testing

PubMed (3)
[See all records that cite these PMIDs]

Help

Summary from all submissions

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

Citations

PubMed

Aberrant 5' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization.

Buratti E, Chivers M, Královicová J, Romano M, Baralle M, Krainer AR, Vorechovsky I.

Nucleic Acids Res. 2007;35(13):4250-63. Epub 2007 Jun 18.

PubMed [citation]
PMID:
17576681
PMCID:
PMC1934990

Statistical features of human exons and their flanking regions.

Zhang MQ.

Hum Mol Genet. 1998 May;7(5):919-32.

PubMed [citation]
PMID:
9536098
See all PubMed Citations (3)

Details of each submission

From Invitae, SCV003304699.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (3)

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. Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. This variant has not been reported in the literature in individuals affected with MUTYH-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant results in the deletion of part of exon 16 (c.1519-84_1596del) of the MUTYH gene. While this variant is not anticipated to result in nonsense mediated decay, it likely alters RNA splicing and results in a disrupted protein product.

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

Last Updated: Feb 20, 2024