NM_001704.3:c.1525+3382A>G

Variant names:

• chr6-68960191-A-G
• rs10485431
• NM_001704.3:c.1525+3382A>G

Variant summary

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

The NM_001704.3(ADGRB3):​c.1525+3382A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.104 in 152,146 control chromosomes in the GnomAD database, including 1,066 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 0.10 (1066 hom., cov: 32)
• Consequence: ADGRB3 NM_001704.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0600
• Publications: 0 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=-0.87).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.149 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ADGRB3	NM_001704.3	c.1525+3382A>G		intron_variant	Intron 8 of 31	ENST00000370598.6	NP_001695.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ADGRB3	ENST00000370598.6	c.1525+3382A>G		intron_variant	Intron 8 of 31	1	NM_001704.3	ENSP00000359630.1
ADGRB3	ENST00000546190.5	c.1525+3382A>G		intron_variant	Intron 6 of 29	1		ENSP00000441821.2
ADGRB3	ENST00000684661.1	n.1525+3382A>G		intron_variant	Intron 8 of 31			ENSP00000507613.1

Frequencies

GnomAD3 genomes AF: 0.104 AC: 15826 AN: 152028 Hom.: 1066 Cov.: 32

Gnomad AFR AF: 0.0272

Gnomad AMI AF: 0.0879

Gnomad AMR AF: 0.0820

Gnomad ASJ AF: 0.0496

Gnomad EAS AF: 0.00963

Gnomad SAS AF: 0.106

Gnomad FIN AF: 0.203

Gnomad MID AF: 0.0570

Gnomad NFE AF: 0.151

Gnomad OTH AF: 0.0948

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

GnomAD4 genome AF: 0.104 AC: 15814 AN: 152146 Hom.: 1066 Cov.: 32 AF XY: 0.105 AC XY: 7834 AN XY: 74342

African (AFR) AF: 0.0271 AC: 1126 AN: 41544

American (AMR) AF: 0.0817 AC: 1247 AN: 15272

Ashkenazi Jewish (ASJ) AF: 0.0496 AC: 172 AN: 3466

East Asian (EAS) AF: 0.00946 AC: 49 AN: 5178

South Asian (SAS) AF: 0.106 AC: 512 AN: 4822

European-Finnish (FIN) AF: 0.203 AC: 2141 AN: 10554

Middle Eastern (MID) AF: 0.0476 AC: 14 AN: 294

European-Non Finnish (NFE) AF: 0.151 AC: 10276 AN: 67996

Other (OTH) AF: 0.0934 AC: 197 AN: 2110

Alfa AF: 0.131 Hom.: 194

Bravo AF: 0.0899

Asia WGS AF: 0.0440 AC: 153 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	0.94
DANN	Benign	0.40
PhyloP100		-0.060
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: rs10485431; hg19: chr6-69670083;