NM_130808.3:c.181-39016C>G

Variant names:

• chr3-131762641-G-C
• rs7612761
• NM_130808.3:c.181-39016C>G

Variant summary

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

The NM_130808.3(CPNE4):​c.181-39016C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0509 in 152,076 control chromosomes in the GnomAD database, including 250 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 0.051 (250 hom., cov: 32)
• Consequence: CPNE4 NM_130808.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.685
• Publications: 0 publications found

Genes affected

CPNE4 (HGNC:2317): (copine 4) This gene belongs to the highly conserved copine family. It encodes a calcium-dependent, phospholipid-binding protein, which may be involved in membrane trafficking, mitogenesis and development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

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 (AFR) allele frequency at 95% confidence interval = 0.0874 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_130808.3. 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
	CPNE4	NM_130808.3	MANE Select	c.181-39016C>G		intron	N/A	NP_570720.1
	CPNE4	NM_001289112.2		c.235-39016C>G		intron	N/A	NP_001276041.1
	CPNE4	NM_153429.2		c.235-39016C>G		intron	N/A	NP_702907.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CPNE4	ENST00000429747.6	TSL:1 MANE Select	c.181-39016C>G		intron	N/A	ENSP00000411904.1
	CPNE4	ENST00000512332.5	TSL:1	c.235-39016C>G		intron	N/A	ENSP00000424853.1
	CPNE4	ENST00000511604.5	TSL:1	c.181-39016C>G		intron	N/A	ENSP00000423811.1

Frequencies

GnomAD3 genomes AF: 0.0509 AC: 7732 AN: 151958 Hom.: 249 Cov.: 32

Gnomad AFR AF: 0.0900

Gnomad AMI AF: 0.0395

Gnomad AMR AF: 0.0363

Gnomad ASJ AF: 0.0184

Gnomad EAS AF: 0.000193

Gnomad SAS AF: 0.0114

Gnomad FIN AF: 0.0287

Gnomad MID AF: 0.0538

Gnomad NFE AF: 0.0424

Gnomad OTH AF: 0.0487

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

GnomAD4 genome AF: 0.0509 AC: 7734 AN: 152076 Hom.: 250 Cov.: 32 AF XY: 0.0477 AC XY: 3543 AN XY: 74338

African (AFR) AF: 0.0898 AC: 3727 AN: 41494

American (AMR) AF: 0.0361 AC: 551 AN: 15246

Ashkenazi Jewish (ASJ) AF: 0.0184 AC: 64 AN: 3470

East Asian (EAS) AF: 0.000193 AC: 1 AN: 5170

South Asian (SAS) AF: 0.0114 AC: 55 AN: 4818

European-Finnish (FIN) AF: 0.0287 AC: 304 AN: 10598

Middle Eastern (MID) AF: 0.0578 AC: 17 AN: 294

European-Non Finnish (NFE) AF: 0.0423 AC: 2877 AN: 67958

Other (OTH) AF: 0.0482 AC: 102 AN: 2116

Alfa AF: 0.0449 Hom.: 20

Bravo AF: 0.0530

Asia WGS AF: 0.00837 AC: 29 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.4
DANN	Benign	0.62
PhyloP100		-0.69
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: rs7612761; hg19: chr3-131481485;