rs2952556

Variant names:

• chr7-121287738-G-A
• rs2952556
• NM_024913.5:c.2869-7702G>A

Variant summary

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

The NM_024913.5(CPED1):​c.2869-7702G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.47 in 151,988 control chromosomes in the GnomAD database, including 18,839 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 0.47 (18839 hom., cov: 32)
• Consequence: CPED1 NM_024913.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.239
• Publications: 5 publications found

Genes affected

CPED1 (HGNC:26159): (cadherin like and PC-esterase domain containing 1) Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.708 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_024913.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CPED1	NM_024913.5	MANE Select	c.2869-7702G>A		intron	N/A	NP_079189.4

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CPED1	ENST00000310396.10	TSL:1 MANE Select	c.2869-7702G>A		intron	N/A	ENSP00000309772.5	A4D0V7-1
	CPED1	ENST00000942586.1		c.2869-7702G>A		intron	N/A	ENSP00000612645.1
	CPED1	ENST00000942583.1		c.2767-7702G>A		intron	N/A	ENSP00000612642.1

Frequencies

GnomAD3 genomes AF: 0.470 AC: 71371 AN: 151870 Hom.: 18809 Cov.: 32

Gnomad AFR AF: 0.714

Gnomad AMI AF: 0.242

Gnomad AMR AF: 0.384

Gnomad ASJ AF: 0.446

Gnomad EAS AF: 0.376

Gnomad SAS AF: 0.562

Gnomad FIN AF: 0.291

Gnomad MID AF: 0.415

Gnomad NFE AF: 0.374

Gnomad OTH AF: 0.463

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

GnomAD4 genome AF: 0.470 AC: 71458 AN: 151988 Hom.: 18839 Cov.: 32 AF XY: 0.463 AC XY: 34369 AN XY: 74296

African (AFR) AF: 0.714 AC: 29617 AN: 41462

American (AMR) AF: 0.383 AC: 5847 AN: 15260

Ashkenazi Jewish (ASJ) AF: 0.446 AC: 1548 AN: 3470

East Asian (EAS) AF: 0.375 AC: 1939 AN: 5164

South Asian (SAS) AF: 0.560 AC: 2697 AN: 4816

European-Finnish (FIN) AF: 0.291 AC: 3074 AN: 10548

Middle Eastern (MID) AF: 0.429 AC: 126 AN: 294

European-Non Finnish (NFE) AF: 0.374 AC: 25395 AN: 67950

Other (OTH) AF: 0.470 AC: 995 AN: 2116

Alfa AF: 0.425 Hom.: 2343

Bravo AF: 0.484

Asia WGS AF: 0.502 AC: 1745 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	2.1
DANN	Benign	0.75
PhyloP100		0.24
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: rs2952556; hg19: chr7-120927792;