rs9925126

Variant names:

• chr16-24026795-A-G
• rs9925126
• NM_002738.7:c.289-5341A>G

Your query was ambiguous. Multiple possible variants found:

• chr16-24026795-A-G
• chr16-24026795-A-T

Variant summary

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

The NM_002738.7(PRKCB):​c.289-5341A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.292 in 152,042 control chromosomes in the GnomAD database, including 6,587 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 0.29 (6587 hom., cov: 32)
• Consequence: PRKCB NM_002738.7 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.30
• Publications: 15 publications found

Genes affected

PRKCB (HGNC:9395): (protein kinase C beta) Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. This protein kinase has been reported to be involved in many different cellular functions, such as B cell activation, apoptosis induction, endothelial cell proliferation, and intestinal sugar absorption. Studies in mice also suggest that this kinase may also regulate neuronal functions and correlate fear-induced conflict behavior after stress. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [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 (NFE) allele frequency at 95% confidence interval = 0.31 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PRKCB	NM_002738.7	c.289-5341A>G		intron_variant	Intron 3 of 16	ENST00000643927.1	NP_002729.2
PRKCB	NM_212535.3	c.289-5341A>G		intron_variant	Intron 3 of 16		NP_997700.1
PRKCB	XM_047434365.1	c.-99-5341A>G		intron_variant	Intron 2 of 15		XP_047290321.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PRKCB	ENST00000643927.1	c.289-5341A>G		intron_variant	Intron 3 of 16		NM_002738.7	ENSP00000496129.1
PRKCB	ENST00000321728.12	c.289-5341A>G		intron_variant	Intron 3 of 16	1		ENSP00000318315.7
PRKCB	ENST00000498739.1	c.-26-65996A>G		intron_variant	Intron 1 of 3	4		ENSP00000459227.1
PRKCB	ENST00000647422.1	n.189-5341A>G		intron_variant	Intron 2 of 4

Frequencies

GnomAD3 genomes AF: 0.292 AC: 44436 AN: 151922 Hom.: 6577 Cov.: 32

Gnomad AFR AF: 0.266

Gnomad AMI AF: 0.315

Gnomad AMR AF: 0.262

Gnomad ASJ AF: 0.454

Gnomad EAS AF: 0.204

Gnomad SAS AF: 0.254

Gnomad FIN AF: 0.301

Gnomad MID AF: 0.392

Gnomad NFE AF: 0.314

Gnomad OTH AF: 0.317

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

GnomAD4 genome AF: 0.292 AC: 44472 AN: 152042 Hom.: 6587 Cov.: 32 AF XY: 0.289 AC XY: 21460 AN XY: 74332

African (AFR) AF: 0.266 AC: 11022 AN: 41470

American (AMR) AF: 0.262 AC: 4001 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.454 AC: 1575 AN: 3466

East Asian (EAS) AF: 0.204 AC: 1055 AN: 5164

South Asian (SAS) AF: 0.256 AC: 1230 AN: 4814

European-Finnish (FIN) AF: 0.301 AC: 3187 AN: 10574

Middle Eastern (MID) AF: 0.405 AC: 119 AN: 294

European-Non Finnish (NFE) AF: 0.314 AC: 21326 AN: 67968

Other (OTH) AF: 0.318 AC: 670 AN: 2104

Alfa AF: 0.305 Hom.: 22087

Bravo AF: 0.288

Asia WGS AF: 0.225 AC: 782 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	0.34
DANN	Benign	0.65
PhyloP100		-1.3
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: rs9925126; hg19: chr16-24038116;