rs2829973

chr21-25888144-A-Gchr21-25888144-A-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_000484.4(APP):c.2211+3578T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.379 in 151,934 control chromosomes in the GnomAD database, including 11,066 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.38 (11066 hom., cov: 31)
• Consequence: APP NM_000484.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.377

Genes affected

APP (HGNC:620): (amyloid beta precursor protein) This gene encodes a cell surface receptor and transmembrane precursor protein that is cleaved by secretases to form a number of peptides. Some of these peptides are secreted and can bind to the acetyltransferase complex APBB1/TIP60 to promote transcriptional activation, while others form the protein basis of the amyloid plaques found in the brains of patients with Alzheimer disease. In addition, two of the peptides are antimicrobial peptides, having been shown to have bacteriocidal and antifungal activities. Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2014]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.43 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
APP	NM_000484.4	c.2211+3578T>C		intron_variant		ENST00000346798.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
APP	ENST00000346798.8	c.2211+3578T>C		intron_variant		1	NM_000484.4

Frequencies

GnomAD3 genomes AF: 0.379 AC: 57477 AN: 151816 Hom.: 11061 Cov.: 31

Gnomad AFR AF: 0.374

Gnomad AMI AF: 0.429

Gnomad AMR AF: 0.306

Gnomad ASJ AF: 0.322

Gnomad EAS AF: 0.145

Gnomad SAS AF: 0.447

Gnomad FIN AF: 0.368

Gnomad MID AF: 0.294

Gnomad NFE AF: 0.415

Gnomad OTH AF: 0.354

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

GnomAD4 genome AF: 0.379 AC: 57512 AN: 151934 Hom.: 11066 Cov.: 31 AF XY: 0.375 AC XY: 27862 AN XY: 74274

Gnomad4 AFR AF: 0.374

Gnomad4 AMR AF: 0.306

Gnomad4 ASJ AF: 0.322

Gnomad4 EAS AF: 0.145

Gnomad4 SAS AF: 0.446

Gnomad4 FIN AF: 0.368

Gnomad4 NFE AF: 0.415

Gnomad4 OTH AF: 0.356

Alfa AF: 0.400 Hom.: 24823

Bravo AF: 0.369

Asia WGS AF: 0.313 AC: 1094 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
Cadd	Benign	0.44
Dann	Benign	0.73

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: rs2829973; hg19: chr21-27260456;