rs786203020

chr5-112839061-AAGAG-Achr5-112839061-AAGAG-AAGchr5-112839061-AAGAG-AAGAGAG

Variant summary

Our verdict is Pathogenic. Variant got 16 ACMG points: 16P and 0B. PVS1 PP5_Very_Strong

The NM_000038.6(APC):c.3471_3474del(p.Glu1157AspfsTer7) variant causes a frameshift change. Variant has been reported in ClinVar as Pathogenic (★★). Synonymous variant affecting the same amino acid position (i.e. E1156E) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: APC NM_000038.6 frameshift
• Clinical Significance: Pathogenic criteria provided, multiple submitters, no conflicts P:5
• Conservation: PhyloP100: 6.89

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 16 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 616 pathogenic variants in the truncated region.
• PP5: Variant 5-112839061-AAGAG-A is Pathogenic according to our data. Variant chr5-112839061-AAGAG-A is described in ClinVar as [Pathogenic]. Clinvar id is 186532.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-112839061-AAGAG-A is described in Lovd as [Pathogenic]. Variant chr5-112839061-AAGAG-A is described in Lovd as [Pathogenic].

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
APC	NM_000038.6	c.3471_3474del	p.Glu1157AspfsTer7	frameshift_variant	16/16	ENST00000257430.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
APC	ENST00000257430.9	c.3471_3474del	p.Glu1157AspfsTer7	frameshift_variant	16/16	5	NM_000038.6	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:5

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

Familial adenomatous polyposis 1 Pathogenic:4

Pathogenic, criteria provided, single submitter	clinical testing	Invitae	Mar 02, 2016	This sequence change deletes 4 nucleotides from exon 16 of the APC mRNA (c.3471_3474delGAGA), causing a frameshift at codon 1157. This creates a premature translational stop signal (p.Glu1157Aspfs*7) and is expected to result in an absent or disrupted protein product. Truncating variants in APC are known to be pathogenic. This particular truncation has been reported in the literature in patients affected with familial adenomatous polyposis (PMID: 10440612, 16676398, 20685668, 17411426, 20223039). For these reasons, this variant has been classified as Pathogenic. -
Pathogenic, criteria provided, single submitter	clinical testing	University of Science and Technology Houari Boumediene, Laboratory of Molecular and Cellular Biology (LBCM)	-	- -
Pathogenic, criteria provided, single submitter	clinical testing	Myriad Genetics, Inc.	May 08, 2023	This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation. -
Pathogenic, criteria provided, single submitter	clinical testing	Invitae	Aug 10, 2023	This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Glu1157Aspfs*7) in the APC gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 1687 amino acid(s) of the APC protein. This premature translational stop signal has been observed in individual(s) with familial adenomatous polyposis (PMID: 10440612, 16676398, 17411426, 20223039, 20685668). ClinVar contains an entry for this variant (Variation ID: 186532). This variant is expected to disrupt the EB1 and HDLG binding sites, which mediate interactions with the cytoskeleton (PMID: 15311282, 17293347). While functional studies have not been performed to directly test the effect on APC protein function, this suggests that disruption of the C-terminal portion of the protein is functionally important. A different truncation (p.Tyr2645Lysfs*14) that lies downstream of this variant has been determined to be pathogenic (PMID: 9824584, 1316610, 27081525, 8381579, 22135120, Invitae). This suggests that deletion of this region of the APC protein is causative of disease. For these reasons, this variant has been classified as Pathogenic. -

Hereditary cancer-predisposing syndrome Pathogenic:1

Pathogenic, criteria provided, single submitter

clinical testing

Ambry Genetics

Jul 30, 2020

The c.3471_3474delGAGA pathogenic mutation, located in coding exon 15 of the APC gene, results from a deletion of 4 nucleotides at nucleotide positions 3471 to 3474, causing a translational frameshift with a predicted alternate stop codon (p.E1157Dfs*7). This mutation has been reported in multiple individuals with a clinical diagnosis of FAP or AFAP (Norheim Andersen S et al. Scand. J. Gastroenterol.,1999 Jun;34:611-7; Friedl W et al. Hered Cancer Clin Pract, 2005 Sep;3:95-114; Soravia C et al. Int J Colorectal Dis, 2006 Jan;21:79-83; Andresen PA et al. J. Cancer Res. Clin. Oncol., 2009 Oct;135:1463-70; Papp J et al. Fam. Cancer, 2016 Jan;15:85-97). In addition to the clinical data presented in the literature, this alteration is expected to result in loss of function by premature protein truncation. As such, 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: rs786203020; hg19: chr5-112174758;