Overview

Variant ID 5156
Entrez Gene ID 26998
Gene FETUB (GeneCards)
Location hg19 3:186376041-186376041
hg38 3:186658252-186658252
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000003.11:g.186376041 G>A (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 198022430

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.2977
CADD Raw score (version 1.3) 0.284623 (Deleterious)
FATHMM raw prediction score 0.10049 (Tolerated)
Deleterious probability by DeFine 0.0842 (Neutral)
Entrez Gene ID 26998 (NCBI Gene)
Official Gene Symbol FETUB (GeneCards)
Number of variants in FETUB in this database 3 (view all the variants)
Full name fetuin B
Band 3q27.3
Other IDs Vega: OTTHUMG00000156586
OMIM: 605954
HGNC: HGNC:3658
Ensembl: ENSG00000090512
Other names 16G2, Gg, IRL685
Summary The protein encoded by this gene is a member of the fetuin family, part of the cystatin superfamily of cysteine protease inhibitors. Fetuins have been implicated in several diverse functions, including osteogenesis and bone resorption, regulation of the insulin and hepatocyte growth factor receptors, and response to systemic inflammation. This protein may be secreted by cells. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.09 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

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;