rs625132

Variant names:

• chr2-31259434-A-G
• rs625132
• NM_014600.3:c.503-1076A>G

Variant summary

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

The NM_014600.3(EHD3):​c.503-1076A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.824 in 152,160 control chromosomes in the GnomAD database, including 51,833 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 0.82 (51833 hom., cov: 31)
• Consequence: EHD3 NM_014600.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.66
• Publications: 12 publications found

Genes affected

EHD3 (HGNC:3244): (EH domain containing 3) Predicted to enable nucleic acid binding activity. Involved in several processes, including Golgi to lysosome transport; endosomal transport; and protein homooligomerization. Acts upstream of or within protein localization to plasma membrane and regulation of cardiac muscle cell membrane potential. Located in ciliary pocket membrane and recycling endosome membrane. [provided by Alliance of Genome Resources, Apr 2022]

LOC124905983 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.927 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_014600.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	EHD3	NM_014600.3	MANE Select	c.503-1076A>G		intron	N/A	NP_055415.1	Q9NZN3-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	EHD3	ENST00000322054.10	TSL:1 MANE Select	c.503-1076A>G		intron	N/A	ENSP00000327116.5	Q9NZN3-1
	EHD3	ENST00000907587.1		c.689-1076A>G		intron	N/A	ENSP00000577646.1
	EHD3	ENST00000907586.1		c.686-1076A>G		intron	N/A	ENSP00000577645.1

Frequencies

GnomAD3 genomes AF: 0.824 AC: 125230 AN: 152042 Hom.: 51797 Cov.: 31

Gnomad AFR AF: 0.765

Gnomad AMI AF: 0.911

Gnomad AMR AF: 0.889

Gnomad ASJ AF: 0.854

Gnomad EAS AF: 0.949

Gnomad SAS AF: 0.933

Gnomad FIN AF: 0.829

Gnomad MID AF: 0.870

Gnomad NFE AF: 0.823

Gnomad OTH AF: 0.843

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

GnomAD4 genome AF: 0.824 AC: 125324 AN: 152160 Hom.: 51833 Cov.: 31 AF XY: 0.828 AC XY: 61625 AN XY: 74386

African (AFR) AF: 0.765 AC: 31745 AN: 41498

American (AMR) AF: 0.889 AC: 13598 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.854 AC: 2962 AN: 3470

East Asian (EAS) AF: 0.950 AC: 4915 AN: 5176

South Asian (SAS) AF: 0.934 AC: 4496 AN: 4814

European-Finnish (FIN) AF: 0.829 AC: 8783 AN: 10596

Middle Eastern (MID) AF: 0.861 AC: 253 AN: 294

European-Non Finnish (NFE) AF: 0.823 AC: 55958 AN: 67996

Other (OTH) AF: 0.845 AC: 1783 AN: 2110

Alfa AF: 0.828 Hom.: 212533

Bravo AF: 0.826

Asia WGS AF: 0.934 AC: 3248 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	0.030
DANN	Benign	0.55
PhyloP100		-1.7
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs625132; hg19: chr2-31482300;