rs3770208

chr2-221419926-C-T

Variant summary

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

The NM_004438.5(EPHA4):c.*1446G>A variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.46 in 152,576 control chromosomes in the GnomAD database, including 16,761 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 0.46 (16716 hom., cov: 33)
  • Exomes 𝑓: 0.41 (45 hom.)
• Consequence: EPHA4 NM_004438.5 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.20

Genes affected

EPHA4 (HGNC:3388): (EPH receptor A4) This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.577 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
EPHA4	NM_004438.5	c.*1446G>A		3_prime_UTR_variant	18/18	ENST00000281821.7
EPHA4	NM_001304536.2	c.*1446G>A		3_prime_UTR_variant	19/19
EPHA4	NM_001304537.2	c.*1446G>A		3_prime_UTR_variant	17/17
EPHA4	NM_001363748.2	c.*1586G>A		3_prime_UTR_variant	18/18

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
EPHA4	ENST00000281821.7	c.*1446G>A		3_prime_UTR_variant	18/18	1	NM_004438.5	P1
EPHA4	ENST00000469354.1	n.994G>A		non_coding_transcript_exon_variant	2/2	2

Frequencies

GnomAD3 genomes AF: 0.460 AC: 69960 AN: 151934 Hom.: 16705 Cov.: 33

Gnomad AFR AF: 0.583

Gnomad AMI AF: 0.446

Gnomad AMR AF: 0.391

Gnomad ASJ AF: 0.390

Gnomad EAS AF: 0.277

Gnomad SAS AF: 0.465

Gnomad FIN AF: 0.454

Gnomad MID AF: 0.497

Gnomad NFE AF: 0.420

Gnomad OTH AF: 0.446

GnomAD4 exome AF: 0.412 AC: 216 AN: 524 Hom.: 45 Cov.: 0 AF XY: 0.437 AC XY: 139 AN XY: 318

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.405

Gnomad4 NFE exome AF: 0.500

Gnomad4 OTH exome AF: 0.300

GnomAD4 genome AF: 0.460 AC: 69999 AN: 152052 Hom.: 16716 Cov.: 33 AF XY: 0.462 AC XY: 34320 AN XY: 74322

Gnomad4 AFR AF: 0.583

Gnomad4 AMR AF: 0.390

Gnomad4 ASJ AF: 0.390

Gnomad4 EAS AF: 0.276

Gnomad4 SAS AF: 0.464

Gnomad4 FIN AF: 0.454

Gnomad4 NFE AF: 0.420

Gnomad4 OTH AF: 0.441

Alfa AF: 0.430 Hom.: 18417

Bravo AF: 0.458

Asia WGS AF: 0.380 AC: 1324 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
Cadd	Benign	1.3
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: rs3770208; hg19: chr2-222284646; COSMIC: COSV56042797; COSMIC: COSV56042797;