chr10-26438309-T-A

Position:

• chr10-26438309-T-A

Variant summary

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

The 10-26438309-T-A variant causes a upstream gene change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.606 in 151,988 control chromosomes in the GnomAD database, including 28,500 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 0.61 (28484 hom., cov: 30)
  • Exomes 𝑓: 0.71 (16 hom.)
• Consequence: APBB1IP NM_019043.4 upstream_gene
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.19

Genes affected

APBB1IP (HGNC:17379): (amyloid beta precursor protein binding family B member 1 interacting protein) Predicted to be involved in signal transduction. Predicted to act upstream of or within T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell and positive regulation of cell adhesion. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.91 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
APBB1IP	NM_019043.4			upstream_gene_variant		ENST00000376236.9
APBB1IP	XM_011519514.3			upstream_gene_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
APBB1IP	ENST00000376236.9			upstream_gene_variant		5	NM_019043.4	P1

Frequencies

GnomAD3 genomes AF: 0.606 AC: 92064 AN: 151808 Hom.: 28459 Cov.: 30

Gnomad AFR AF: 0.518

Gnomad AMI AF: 0.635

Gnomad AMR AF: 0.614

Gnomad ASJ AF: 0.566

Gnomad EAS AF: 0.933

Gnomad SAS AF: 0.803

Gnomad FIN AF: 0.696

Gnomad MID AF: 0.652

Gnomad NFE AF: 0.607

Gnomad OTH AF: 0.601

GnomAD4 exome AF: 0.710 AC: 44 AN: 62 Hom.: 16 Cov.: 0 AF XY: 0.727 AC XY: 32 AN XY: 44

Gnomad4 EAS exome AF: 1.00

Gnomad4 FIN exome AF: 0.500

Gnomad4 NFE exome AF: 0.682

Gnomad4 OTH exome AF: 0.833

GnomAD4 genome AF: 0.606 AC: 92130 AN: 151926 Hom.: 28484 Cov.: 30 AF XY: 0.617 AC XY: 45822 AN XY: 74220

Gnomad4 AFR AF: 0.518

Gnomad4 AMR AF: 0.615

Gnomad4 ASJ AF: 0.566

Gnomad4 EAS AF: 0.932

Gnomad4 SAS AF: 0.803

Gnomad4 FIN AF: 0.696

Gnomad4 NFE AF: 0.607

Gnomad4 OTH AF: 0.604

Alfa AF: 0.607 Hom.: 3486

Bravo AF: 0.595

Asia WGS AF: 0.829 AC: 2880 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	0.20
DANN	Benign	0.68

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: rs1335540; hg19: chr10-26727238;