NM_001704.3:c.2608-268C>T

Variant names:

• chr6-69234764-C-T
• rs779462
• NM_001704.3:c.2608-268C>T

Variant summary

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

The NM_001704.3(ADGRB3):​c.2608-268C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0731 in 151,994 control chromosomes in the GnomAD database, including 563 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 0.073 (563 hom., cov: 32)
• Consequence: ADGRB3 NM_001704.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0830
• Publications: 2 publications found

Genes affected

ADGRB3 (HGNC:945): (adhesion G protein-coupled receptor B3) This p53-target gene encodes a brain-specific angiogenesis inhibitor, a seven-span transmembrane protein, and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities, and may also play a role in angiogenesis. [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=-0.83).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.104 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001704.3. 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
	ADGRB3	NM_001704.3	MANE Select	c.2608-268C>T		intron	N/A	NP_001695.2	O60242-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ADGRB3	ENST00000370598.6	TSL:1 MANE Select	c.2608-268C>T		intron	N/A	ENSP00000359630.1	O60242-1
	ADGRB3	ENST00000546190.5	TSL:1	c.2608-268C>T		intron	N/A	ENSP00000441821.2	O60242-1
	ADGRB3	ENST00000238918.12	TSL:2	c.226-268C>T		intron	N/A	ENSP00000238918.8	J3KMY8

Frequencies

GnomAD3 genomes AF: 0.0731 AC: 11107 AN: 151876 Hom.: 562 Cov.: 32

Gnomad AFR AF: 0.0194

Gnomad AMI AF: 0.0768

Gnomad AMR AF: 0.0679

Gnomad ASJ AF: 0.0979

Gnomad EAS AF: 0.00116

Gnomad SAS AF: 0.0849

Gnomad FIN AF: 0.0977

Gnomad MID AF: 0.0854

Gnomad NFE AF: 0.107

Gnomad OTH AF: 0.0738

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

GnomAD4 genome AF: 0.0731 AC: 11104 AN: 151994 Hom.: 563 Cov.: 32 AF XY: 0.0713 AC XY: 5296 AN XY: 74278

African (AFR) AF: 0.0193 AC: 801 AN: 41510

American (AMR) AF: 0.0678 AC: 1034 AN: 15252

Ashkenazi Jewish (ASJ) AF: 0.0979 AC: 339 AN: 3462

East Asian (EAS) AF: 0.00116 AC: 6 AN: 5164

South Asian (SAS) AF: 0.0850 AC: 409 AN: 4814

European-Finnish (FIN) AF: 0.0977 AC: 1032 AN: 10562

Middle Eastern (MID) AF: 0.0918 AC: 27 AN: 294

European-Non Finnish (NFE) AF: 0.106 AC: 7232 AN: 67916

Other (OTH) AF: 0.0731 AC: 154 AN: 2108

Alfa AF: 0.0830 Hom.: 108

Bravo AF: 0.0681

Asia WGS AF: 0.0300 AC: 104 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	0.60
DANN	Benign	0.47
PhyloP100		-0.083
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: rs779462; hg19: chr6-69944656;