rs764830

chr4-113696659-G-Achr4-113696659-G-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001321571.2(CAMK2D):c.161-34887C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.706 in 151,990 control chromosomes in the GnomAD database, including 38,734 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 0.71 (38734 hom., cov: 31)
• Consequence: CAMK2D NM_001321571.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0390

Genes affected

CAMK2D (HGNC:1462): (calcium/calmodulin dependent protein kinase II delta) The product of this gene belongs to the serine/threonine protein kinase family and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. In mammalian cells, the enzyme is composed of four different chains: alpha, beta, gamma, and delta. The product of this gene is a delta chain. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Distinct isoforms of this chain have different expression patterns.[provided by RefSeq, Nov 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.844 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CAMK2D	NM_001321571.2	c.161-34887C>T		intron_variant		ENST00000511664.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CAMK2D	ENST00000511664.6	c.161-34887C>T		intron_variant		2	NM_001321571.2

Frequencies

GnomAD3 genomes AF: 0.705 AC: 107140 AN: 151872 Hom.: 38663 Cov.: 31

Gnomad AFR AF: 0.851

Gnomad AMI AF: 0.668

Gnomad AMR AF: 0.722

Gnomad ASJ AF: 0.632

Gnomad EAS AF: 0.746

Gnomad SAS AF: 0.661

Gnomad FIN AF: 0.727

Gnomad MID AF: 0.674

Gnomad NFE AF: 0.615

Gnomad OTH AF: 0.688

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

GnomAD4 genome AF: 0.706 AC: 107276 AN: 151990 Hom.: 38734 Cov.: 31 AF XY: 0.711 AC XY: 52816 AN XY: 74282

Gnomad4 AFR AF: 0.851

Gnomad4 AMR AF: 0.722

Gnomad4 ASJ AF: 0.632

Gnomad4 EAS AF: 0.747

Gnomad4 SAS AF: 0.662

Gnomad4 FIN AF: 0.727

Gnomad4 NFE AF: 0.615

Gnomad4 OTH AF: 0.689

Alfa AF: 0.631 Hom.: 40098

Bravo AF: 0.712

Asia WGS AF: 0.739 AC: 2574 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
Cadd	Benign	1.5
Dann	Benign	0.74

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

Publications

LitVar

Other links and lift over

dbSNP: rs764830; hg19: chr4-114617815; COSMIC: COSV56440039;