rs135764

Positions:

• chr22-38314407-G-A
• chr22-38314407-G-C

Variant summary

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

The NM_152221.3(CSNK1E):​c.-12-238C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0706 in 152,264 control chromosomes in the GnomAD database, including 461 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 0.071 (461 hom., cov: 33)
• Consequence: CSNK1E NM_152221.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0690

Genes affected

CSNK1E (HGNC:2453): (casein kinase 1 epsilon) The protein encoded by this gene is a serine/threonine protein kinase and a member of the casein kinase I protein family, whose members have been implicated in the control of cytoplasmic and nuclear processes, including DNA replication and repair. The encoded protein is found in the cytoplasm as a monomer and can phosphorylate a variety of proteins, including itself. This protein has been shown to phosphorylate period, a circadian rhythm protein. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2014]

TPTEP2-CSNK1E (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.156 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CSNK1E	NM_152221.3	c.-12-238C>T		intron_variant		ENST00000396832.6	NP_689407.1
TPTEP2-CSNK1E	NM_001289912.2	c.-12-238C>T		intron_variant			NP_001276841.1
CSNK1E	NM_001894.5	c.-12-238C>T		intron_variant			NP_001885.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CSNK1E	ENST00000396832.6	c.-12-238C>T		intron_variant		1	NM_152221.3	ENSP00000380044	P1

Frequencies

GnomAD3 genomes AF: 0.0706 AC: 10748 AN: 152146 Hom.: 459 Cov.: 33

Gnomad AFR AF: 0.0191

Gnomad AMI AF: 0.0362

Gnomad AMR AF: 0.0673

Gnomad ASJ AF: 0.0746

Gnomad EAS AF: 0.165

Gnomad SAS AF: 0.128

Gnomad FIN AF: 0.104

Gnomad MID AF: 0.0791

Gnomad NFE AF: 0.0862

Gnomad OTH AF: 0.0805

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

GnomAD4 genome AF: 0.0706 AC: 10743 AN: 152264 Hom.: 461 Cov.: 33 AF XY: 0.0714 AC XY: 5312 AN XY: 74446

Gnomad4 AFR AF: 0.0190

Gnomad4 AMR AF: 0.0673

Gnomad4 ASJ AF: 0.0746

Gnomad4 EAS AF: 0.165

Gnomad4 SAS AF: 0.127

Gnomad4 FIN AF: 0.104

Gnomad4 NFE AF: 0.0862

Gnomad4 OTH AF: 0.0829

Alfa AF: 0.0673 Hom.: 121

Bravo AF: 0.0659

Asia WGS AF: 0.166 AC: 576 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	2.1
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: rs135764; hg19: chr22-38710412;