Variant ID | 23761 |
---|---|
Entrez Gene ID | 866 |
Gene | SERPINA6 (GeneCards) |
Location | hg19 14:94785774-94785774
hg38 14:94319437-94319437 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000014.8:g.94785774 A>G (Genome Assembly: GRCh37) |
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 | 107349540 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
EIGEN score | -0.2081 |
CADD Raw score (version 1.3) | 0.375033 (Deleterious) |
FATHMM raw prediction score | 0.07999 (Tolerated) |
Deleterious probability by DeFine | 0.0906 (Neutral) |
Entrez Gene ID | 866 (NCBI Gene) |
---|---|
Official Gene Symbol | SERPINA6 (GeneCards) |
Number of variants in SERPINA6 in this database | 5 (view all the variants) |
Full name | serpin family A member 6 |
Band | 14q32.13 |
Other IDs | Vega: OTTHUMG00000171346 OMIM: 122500 HGNC: HGNC:1540 Ensembl: ENSG00000170099 |
Other names | CBG |
Summary | This gene encodes an alpha-globulin protein with corticosteroid-binding properties. This is the major transport protein for glucorticoids and progestins in the blood of most vertebrates. The gene localizes to a chromosomal region containing several closely related serine protease inhibitors which may have evolved by duplication events. [provided by RefSeq, Jul 2008] |
Individual ID | 29217587.01 (view all the variants in this individual) |
---|---|
Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
---|---|
Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
Journal | Science |
Publication date | 2018.02 |
Disease | Asymptomatic |
Number of cases | cases of unknown sex: 3; |