NM_153634.3:c.186+8157T>C

Variant names:

• chr12-38864847-A-G
• rs10876185
• NM_153634.3:c.186+8157T>C

Variant summary

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

The NM_153634.3(CPNE8):​c.186+8157T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.135 in 152,180 control chromosomes in the GnomAD database, including 2,230 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 0.14 (2230 hom., cov: 32)
• Consequence: CPNE8 NM_153634.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.504
• Publications: 2 publications found

Genes affected

CPNE8 (HGNC:23498): (copine 8) Calcium-dependent membrane-binding proteins may regulate molecular events at the interface of the cell membrane and cytoplasm. This gene is one of several genes that encode a calcium-dependent protein containing two N-terminal type II C2 domains and an integrin A domain-like sequence in the C-terminus. [provided by RefSeq, Jul 2008]

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 = 0.295 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CPNE8	NM_153634.3	c.186+8157T>C		intron_variant	Intron 3 of 19	ENST00000331366.10	NP_705898.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CPNE8	ENST00000331366.10	c.186+8157T>C		intron_variant	Intron 3 of 19	1	NM_153634.3	ENSP00000329748.5
CPNE8	ENST00000360449.3	c.150+8157T>C		intron_variant	Intron 3 of 19	2		ENSP00000353633.3
CPNE8	ENST00000550863.1	c.-298+8157T>C		intron_variant	Intron 3 of 7	4		ENSP00000447761.1

Frequencies

GnomAD3 genomes AF: 0.135 AC: 20533 AN: 152062 Hom.: 2229 Cov.: 32

Gnomad AFR AF: 0.299

Gnomad AMI AF: 0.0230

Gnomad AMR AF: 0.0804

Gnomad ASJ AF: 0.0724

Gnomad EAS AF: 0.268

Gnomad SAS AF: 0.0757

Gnomad FIN AF: 0.0359

Gnomad MID AF: 0.0728

Gnomad NFE AF: 0.0624

Gnomad OTH AF: 0.124

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

GnomAD4 genome AF: 0.135 AC: 20560 AN: 152180 Hom.: 2230 Cov.: 32 AF XY: 0.132 AC XY: 9822 AN XY: 74422

African (AFR) AF: 0.299 AC: 12401 AN: 41466

American (AMR) AF: 0.0802 AC: 1227 AN: 15300

Ashkenazi Jewish (ASJ) AF: 0.0724 AC: 251 AN: 3466

East Asian (EAS) AF: 0.268 AC: 1388 AN: 5184

South Asian (SAS) AF: 0.0761 AC: 367 AN: 4820

European-Finnish (FIN) AF: 0.0359 AC: 381 AN: 10618

Middle Eastern (MID) AF: 0.0714 AC: 21 AN: 294

European-Non Finnish (NFE) AF: 0.0624 AC: 4243 AN: 68006

Other (OTH) AF: 0.123 AC: 260 AN: 2114

Alfa AF: 0.0333 Hom.: 29

Bravo AF: 0.147

Asia WGS AF: 0.166 AC: 575 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	4.4
DANN	Benign	0.69
PhyloP100		0.50
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: rs10876185; hg19: chr12-39258649;