chr3-134981345-C-T

Variant names:

• chr3-134981345-C-T
• rs36110
• NM_004441.5:c.805+29293C>T

Variant summary

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

The NM_004441.5(EPHB1):​c.805+29293C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.631 in 152,070 control chromosomes in the GnomAD database, including 32,090 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 0.63 (32090 hom., cov: 32)
• Consequence: EPHB1 NM_004441.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.28
• Publications: 7 publications found

Genes affected

EPHB1 (HGNC:3392): (EPH receptor B1) Ephrin receptors and their ligands, the ephrins, mediate numerous developmental processes, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of 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. Ephrin receptors make up the largest subgroup of the receptor tyrosine kinase (RTK) family. The protein encoded by this gene is a receptor for ephrin-B family members. [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=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.822 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
EPHB1	NM_004441.5	c.805+29293C>T		intron_variant	Intron 3 of 15	ENST00000398015.8	NP_004432.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
EPHB1	ENST00000398015.8	c.805+29293C>T		intron_variant	Intron 3 of 15	1	NM_004441.5	ENSP00000381097.3
EPHB1	ENST00000482618.5	n.*71+3268C>T		intron_variant	Intron 4 of 5	1		ENSP00000420338.1
EPHB1	ENST00000488154.5	n.471+29627C>T		intron_variant	Intron 3 of 4	1
EPHB1	ENST00000647596.1	c.805+29293C>T		intron_variant	Intron 3 of 15			ENSP00000497153.1

Frequencies

GnomAD3 genomes AF: 0.631 AC: 95858 AN: 151948 Hom.: 32049 Cov.: 32

Gnomad AFR AF: 0.829

Gnomad AMI AF: 0.656

Gnomad AMR AF: 0.532

Gnomad ASJ AF: 0.642

Gnomad EAS AF: 0.152

Gnomad SAS AF: 0.485

Gnomad FIN AF: 0.515

Gnomad MID AF: 0.696

Gnomad NFE AF: 0.596

Gnomad OTH AF: 0.642

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

GnomAD4 genome AF: 0.631 AC: 95946 AN: 152070 Hom.: 32090 Cov.: 32 AF XY: 0.620 AC XY: 46130 AN XY: 74358

African (AFR) AF: 0.829 AC: 34401 AN: 41492

American (AMR) AF: 0.531 AC: 8121 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.642 AC: 2229 AN: 3472

East Asian (EAS) AF: 0.153 AC: 790 AN: 5176

South Asian (SAS) AF: 0.485 AC: 2334 AN: 4814

European-Finnish (FIN) AF: 0.515 AC: 5435 AN: 10556

Middle Eastern (MID) AF: 0.704 AC: 207 AN: 294

European-Non Finnish (NFE) AF: 0.596 AC: 40495 AN: 67960

Other (OTH) AF: 0.634 AC: 1337 AN: 2108

Alfa AF: 0.626 Hom.: 4011

Bravo AF: 0.638

Asia WGS AF: 0.374 AC: 1302 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.21
DANN	Benign	0.74
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: rs36110; hg19: chr3-134700187;