NM_004307.2:c.1529+4390T>G

Variant names:

• chr4-40885974-A-C
• rs16852584
• NM_004307.2:c.1529+4390T>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_004307.2(APBB2):​c.1529+4390T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0688 in 152,098 control chromosomes in the GnomAD database, including 429 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 0.069 (429 hom., cov: 32)
• Consequence: APBB2 NM_004307.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.21
• Publications: 4 publications found

Genes affected

APBB2 (HGNC:582): (amyloid beta precursor protein binding family B member 2) The protein encoded by this gene interacts with the cytoplasmic domains of amyloid beta (A4) precursor protein and amyloid beta (A4) precursor-like protein 2. This protein contains two phosphotyrosine binding (PTB) domains, which are thought to function in signal transduction. Polymorphisms in this gene have been associated with Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.104 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_004307.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	APBB2	NM_004307.2	MANE Select	c.1529+4390T>G		intron	N/A	NP_004298.1
	APBB2	NM_001166050.2		c.1526+4390T>G		intron	N/A	NP_001159522.1
	APBB2	NM_001330656.2		c.1463+4390T>G		intron	N/A	NP_001317585.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	APBB2	ENST00000508593.6	TSL:1 MANE Select	c.1529+4390T>G		intron	N/A	ENSP00000427211.1
	APBB2	ENST00000513140.5	TSL:1	c.1463+4390T>G		intron	N/A	ENSP00000426018.1
	APBB2	ENST00000295974.12	TSL:2	c.1526+4390T>G		intron	N/A	ENSP00000295974.8

Frequencies

GnomAD3 genomes AF: 0.0689 AC: 10468 AN: 151980 Hom.: 430 Cov.: 32

Gnomad AFR AF: 0.0770

Gnomad AMI AF: 0.00219

Gnomad AMR AF: 0.0719

Gnomad ASJ AF: 0.129

Gnomad EAS AF: 0.112

Gnomad SAS AF: 0.0290

Gnomad FIN AF: 0.0962

Gnomad MID AF: 0.123

Gnomad NFE AF: 0.0557

Gnomad OTH AF: 0.0847

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

GnomAD4 genome AF: 0.0688 AC: 10462 AN: 152098 Hom.: 429 Cov.: 32 AF XY: 0.0698 AC XY: 5187 AN XY: 74350

African (AFR) AF: 0.0769 AC: 3190 AN: 41488

American (AMR) AF: 0.0718 AC: 1097 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.129 AC: 446 AN: 3470

East Asian (EAS) AF: 0.111 AC: 576 AN: 5174

South Asian (SAS) AF: 0.0292 AC: 140 AN: 4794

European-Finnish (FIN) AF: 0.0962 AC: 1016 AN: 10564

Middle Eastern (MID) AF: 0.112 AC: 33 AN: 294

European-Non Finnish (NFE) AF: 0.0557 AC: 3785 AN: 68008

Other (OTH) AF: 0.0838 AC: 177 AN: 2112

Alfa AF: 0.0616 Hom.: 593

Bravo AF: 0.0709

Asia WGS AF: 0.0590 AC: 204 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	5.5
DANN	Benign	0.64
PhyloP100		1.2
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs16852584; hg19: chr4-40887991;