Overview

Variant ID 32555
Entrez Gene ID 577
Gene BAI3 (GeneCards)
Location hg19 6:69646515-69646515
hg38 6:68936623-68936623
Disease Asymptomatic
Method NGS gene panel
Mutation(HGVS format) NC_000006.11:g.69646515 C>A (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 325
Amino acid changes in protein H > N
Position in cDNA 973
Changes in cDNA C > A
mRNA accession NA
mRNA length NA
Reference length 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
Variant IDs in COSMIC (version 89) 229010
Variant occurences in COSMIC 1(skin)
EIGEN score 0.2293
CADD Raw score (version 1.3) 4.445399 (Deleterious)
FATHMM raw prediction score 0.96524 (Tolerated)
SIFT score 0.184 (Tolerated)
LRT score 0 (Deleterious)
MutationTaster score 0.999 (Deleterious)
MutatioinAssessor score -0.25 (Tolerated)
PROVEAN score -1.04 (Tolerated)
MetaSVM score -1.087 (Tolerated)
MetaLR score 0.047 (Tolerated)
MCAP score 0.012 (Tolerated)
FitCons score 0.554 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.42
PhyloP score based on multiple alignment of 100 vertebrates 6.16
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 19.224
Deleterious probability by iFish2 0.4502 (Neutral)
Deleterious probability by DeFine 0.9673 (Deleterious)
Entrez Gene ID 577 (NCBI Gene)
Official Gene Symbol BAI3 (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 25999502.02 (view all the variants in this individual)
Pubmed ID 25999502
Whose mosaic mutation Normal  
Origin of mosaic mutation in patients de novo
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 25999502

Pubmed ID 25999502
Title High burden and pervasive positive selection of somatic mutations in normal human skin
Journal Science
Publication date 2015.05
Disease Asymptomatic
Number of cases Male cases: 1; Female cases: 3;