Overview

Variant ID 10284
Entrez Gene ID 577
Gene ADGRB3 (GeneCards)
Location hg19 6:70372530-70372530
hg38 6:69662638-69662638
Disease Xeroderma Pigmentosum (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000006.11:g.70372530 T>C (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.1374
CADD Raw score (version 1.3) 0.121396 (Deleterious)
FATHMM raw prediction score 0.16357 (Tolerated)
Deleterious probability by DeFine 0.2731 (Neutral)
Entrez Gene ID 577 (NCBI Gene)
Official Gene Symbol ADGRB3 (GeneCards)
Number of variants in ADGRB3 in this database 111 (view all the variants)
Full name adhesion G protein-coupled receptor B3
Band 6q12-q13
Other IDs Vega: OTTHUMG00000014982
OMIM: 602684
HGNC: HGNC:945
Ensembl: ENSG00000135298
Other names BAI3
Summary 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]

Individual #1

Individual ID 29217584.23 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Xeroderma Pigmentosum (view all the variants in this disease)
OMIM ID 278700

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;