rs863225358

Positions:

• chr5-112840242-GAGAA-G

Variant summary

Our verdict is Pathogenic. Variant got 18 ACMG points: 18P and 0B. PVS1 PM2 PP5_Very_Strong

The NM_000038.6(APC):​c.4652_4655del​(p.Lys1551ArgfsTer13) variant causes a frameshift change. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (★★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: APC NM_000038.6 frameshift
• Clinical Significance: Pathogenic criteria provided, multiple submitters, no conflicts P:3
• Conservation: PhyloP100: 7.15

Genes affected

APC (HGNC:583): (APC regulator of WNT signaling pathway) This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Mutations in the APC gene have been found to occur in most colorectal cancers, where disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. [provided by RefSeq, Jun 2022]

ACMG classification

Verdict is Pathogenic. Variant got 18 ACMG points.

• PVS1: Loss of function variant, product does not undergo nonsense mediated mRNA decay. Variant is located in the 3'-most exon, not predicted to undergo nonsense mediated mRNA decay. There are 25 pathogenic variants in the truncated region.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 5-112840242-GAGAA-G is Pathogenic according to our data. Variant chr5-112840242-GAGAA-G is described in ClinVar as [Pathogenic]. Clinvar id is 217987.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-112840242-GAGAA-G is described in Lovd as [Pathogenic].

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
APC	NM_000038.6	c.4652_4655del	p.Lys1551ArgfsTer13	frameshift_variant	16/16	ENST00000257430.9	NP_000029.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
APC	ENST00000257430.9	c.4652_4655del	p.Lys1551ArgfsTer13	frameshift_variant	16/16	5	NM_000038.6	ENSP00000257430	P1

Frequencies

GnomAD3 genomes Cov.: 32

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome Cov.: 32

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:3

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

Familial adenomatous polyposis 1 Pathogenic:1

Pathogenic, criteria provided, single submitter

clinical testing

Myriad Genetics, Inc.

May 11, 2023

This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation. -

not provided Pathogenic:1

Pathogenic, no assertion criteria provided

research

Mayo Clinic Laboratories, Mayo Clinic

-

- -

Hereditary cancer-predisposing syndrome Pathogenic:1

Pathogenic, criteria provided, single submitter

clinical testing

Ambry Genetics

Dec 29, 2021

The c.4652_4655delAAGA pathogenic mutation, located in coding exon 15 of the APC gene, results from a deletion of 4 nucleotides between positions 4652 and 4655, causing a translational frameshift with a predicted alternate stop codon (p.K1551Rfs*13). This alteration occurs at the 3' terminus of theAPC gene, is not expected to trigger nonsense-mediated mRNA decay, and impacts the last 1293 amino acids of the protein. However, premature stop codons are typically deleterious in nature a significant portion of the protein is affected (Ambry internal data). This alteration was first reported as a 4 bp deletion at codon 1552 in a German family affected with familial adenomatous polyposis (FAP) (Mandl M et al. Hum Mol Genet. 1994 Jan;3(1):181-4). This alteration has since been identified by another study in 2 individuals from a cohort of 1166 unrelated German patients with a clinical diagnosis of FAP or multiple adenomatous polyposis consistent with attenuated FAP (AFAP) (Friedl W et al. Hered Cancer Clin Pract. 2005 Sep 15;3(3):95-114). An additional study detected this alteration in 2 of 1591 consecutive patients referred for molecular analysis of APC due to suspected FAP at the Mayo Clinic. The authors note that these individuals were affected with AFAP, epidermal cysts and supernumerary teeth (Kerr S et al. J Mol Diagn. 2013 Jan;15(1):31-43). This variant is considered to be rare based on population cohorts in the Genome Aggregation Database (gnomAD). Based on the supporting evidence, this alteration is interpreted as a disease-causing mutation. -

Computational scores

Source: dbNSFP v4.3

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs863225358; hg19: chr5-112175939;