| Variant ID | 32569 |
|---|---|
| Entrez Gene ID | 577 |
| Gene | BAI3 (GeneCards) |
| Location | hg19 6:70070991-70070991
hg38 6:69361099-69361099 |
| Disease | Asymptomatic |
| Method | NGS gene panel |
| Mutation(HGVS format) | NC_000006.11:g.70070991 G>T (Genome Assembly: hg19) |
| Exon or Intron | Exon |
|---|---|
| Position in protein | 1276 |
| Amino acid changes in protein | E > * |
| Position in cDNA | 3826 |
| Changes in cDNA | G > T |
| mRNA accession | NA |
| mRNA length | NA |
| Reference length | 171115067 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 1.0012 |
| CADD Raw score (version 1.3) | 15.147554 (Deleterious) |
| FATHMM raw prediction score | 0.99636 (Tolerated) |
| LRT score | 0 (Deleterious) |
| MutationTaster score | 1 (Deleterious) |
| FitCons score | 0.554 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | 5.34 |
| PhyloP score based on multiple alignment of 100 vertebrates | 9.27 |
| PhastCons score based on multiple alignment of 100 vertebrates | 1 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 19.394 |
| Deleterious probability by DeFine | 0.9414 (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 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 |
| 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; |