rs1457115

chr5-111231900-C-T

Variant summary

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

The NM_001744.6(CAMK4):c.161+7256C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.444 in 151,974 control chromosomes in the GnomAD database, including 15,226 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 0.44 (15226 hom., cov: 32)
• Consequence: CAMK4 NM_001744.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.174

Genes affected

CAMK4 (HGNC:1464): (calcium/calmodulin dependent protein kinase IV) The product of this gene belongs to the serine/threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. This enzyme is a multifunctional serine/threonine protein kinase with limited tissue distribution, that has been implicated in transcriptional regulation in lymphocytes, neurons and male germ cells. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.75).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.48 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CAMK4	NM_001744.6	c.161+7256C>T		intron_variant		ENST00000282356.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CAMK4	ENST00000282356.9	c.161+7256C>T		intron_variant		1	NM_001744.6	P1

Frequencies

GnomAD3 genomes AF: 0.444 AC: 67427 AN: 151856 Hom.: 15218 Cov.: 32

Gnomad AFR AF: 0.486

Gnomad AMI AF: 0.556

Gnomad AMR AF: 0.366

Gnomad ASJ AF: 0.392

Gnomad EAS AF: 0.244

Gnomad SAS AF: 0.417

Gnomad FIN AF: 0.403

Gnomad MID AF: 0.415

Gnomad NFE AF: 0.461

Gnomad OTH AF: 0.452

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

GnomAD4 genome AF: 0.444 AC: 67452 AN: 151974 Hom.: 15226 Cov.: 32 AF XY: 0.439 AC XY: 32620 AN XY: 74274

Gnomad4 AFR AF: 0.486

Gnomad4 AMR AF: 0.365

Gnomad4 ASJ AF: 0.392

Gnomad4 EAS AF: 0.243

Gnomad4 SAS AF: 0.416

Gnomad4 FIN AF: 0.403

Gnomad4 NFE AF: 0.461

Gnomad4 OTH AF: 0.451

Alfa AF: 0.458 Hom.: 21838

Bravo AF: 0.445

Asia WGS AF: 0.327 AC: 1139 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.75
Cadd	Benign	2.2
Dann	Benign	0.51

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: rs1457115; hg19: chr5-110567598;