Variant ID | 33744 |
---|---|
Entrez Gene ID | 577 |
Gene | BAI3 (GeneCards) |
Location | hg19 6:69703822-69703822
hg38 6:68993930-68993930 |
Disease | Asymptomatic |
Method | NGS gene panel |
Mutation(HGVS format) | NC_000006.11:g.69703822 G>A (Genome Assembly: hg19) |
Exon or Intron | Exon |
---|---|
Position in protein | 633 |
Amino acid changes in protein | A > T |
Position in cDNA | 1897 |
Changes in cDNA | G > A |
mRNA accession | NA |
mRNA length | NA |
Reference length | 171115067 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.9326 |
CADD Raw score (version 1.3) | 5.598988 (Deleterious) |
FATHMM raw prediction score | 0.99145 (Tolerated) |
SIFT score | 0.03 (Deleterious) |
LRT score | 0 (Deleterious) |
MutationTaster score | 1 (Deleterious) |
MutatioinAssessor score | 1.365 (Tolerated) |
PROVEAN score | -2.69 (Deleterious) |
MetaSVM score | -1.184 (Tolerated) |
MetaLR score | 0.063 (Tolerated) |
MCAP score | 0.043 (Deleterious) |
FitCons score | 0.554 (Highly Significant p < 0.003 ) |
Genomic Evolutionary Rate Profiling (GERP) score | 6.05 |
PhyloP score based on multiple alignment of 100 vertebrates | 10.003 |
PhastCons score based on multiple alignment of 100 vertebrates | 1 |
SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 20.601 |
Deleterious probability by iFish2 | 0.9842 (Deleterious) |
Deleterious probability by DeFine | 0.9558 (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 | 25999502.03 (view all the variants in this individual) |
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Pubmed ID | 25999502 |
Whose mosaic mutation | Normal |
Origin of mosaic mutation in patients | de novo |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 25999502 |
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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; |