rs12155789

Variant names:

• chr8-22786194-A-G
• rs12155789
• NM_144962.3:c.357+31443T>C

Variant summary

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

The NM_144962.3(PEBP4):​c.357+31443T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.123 in 152,124 control chromosomes in the GnomAD database, including 1,255 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 0.12 (1255 hom., cov: 32)
• Consequence: PEBP4 NM_144962.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.896
• Publications: 4 publications found

Genes affected

PEBP4 (HGNC:28319): (phosphatidylethanolamine binding protein 4) The phosphatidylethanolamine (PE)-binding proteins, including PEBP4, are an evolutionarily conserved family of proteins with pivotal biologic functions, such as lipid binding and inhibition of serine proteases (Wang et al., 2004 [PubMed 15302887]).[supplied by OMIM, Dec 2008]

ENSG00000253125 (HGNC:58186):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.163 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PEBP4	NM_144962.3	c.357+31443T>C		intron_variant	Intron 4 of 6	ENST00000256404.8	NP_659399.2
PEBP4	NM_001363233.2	c.357+31443T>C		intron_variant	Intron 4 of 6		NP_001350162.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PEBP4	ENST00000256404.8	c.357+31443T>C		intron_variant	Intron 4 of 6	1	NM_144962.3	ENSP00000256404.6
ENSG00000253125	ENST00000523627.1	n.490-12342A>G		intron_variant	Intron 4 of 4	4

Frequencies

GnomAD3 genomes AF: 0.123 AC: 18662 AN: 152006 Hom.: 1256 Cov.: 32

Gnomad AFR AF: 0.0658

Gnomad AMI AF: 0.138

Gnomad AMR AF: 0.106

Gnomad ASJ AF: 0.0900

Gnomad EAS AF: 0.0868

Gnomad SAS AF: 0.0728

Gnomad FIN AF: 0.141

Gnomad MID AF: 0.139

Gnomad NFE AF: 0.166

Gnomad OTH AF: 0.132

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

GnomAD4 genome AF: 0.123 AC: 18656 AN: 152124 Hom.: 1255 Cov.: 32 AF XY: 0.120 AC XY: 8895 AN XY: 74350

African (AFR) AF: 0.0657 AC: 2728 AN: 41520

American (AMR) AF: 0.106 AC: 1619 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.0900 AC: 312 AN: 3466

East Asian (EAS) AF: 0.0870 AC: 450 AN: 5174

South Asian (SAS) AF: 0.0726 AC: 349 AN: 4804

European-Finnish (FIN) AF: 0.141 AC: 1484 AN: 10562

Middle Eastern (MID) AF: 0.129 AC: 38 AN: 294

European-Non Finnish (NFE) AF: 0.166 AC: 11274 AN: 67988

Other (OTH) AF: 0.131 AC: 276 AN: 2110

Alfa AF: 0.149 Hom.: 3094

Bravo AF: 0.121

Asia WGS AF: 0.0700 AC: 242 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.10
DANN	Benign	0.42
PhyloP100		-0.90
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: rs12155789; hg19: chr8-22643707;