Overview

Variant ID 10057
Entrez Gene ID 26036
Gene ZNF451 (GeneCards)
Location hg19 6:56954559-56954559
hg38 6:57089761-57089761
Disease Cockayne syndrome (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000006.11:g.56954559 C>G (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 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.4283
CADD Raw score (version 1.3) 0.504319 (Deleterious)
FATHMM raw prediction score 0.34255 (Tolerated)
Deleterious probability by DeFine 0.6155 (Deleterious)
Entrez Gene ID 26036 (NCBI Gene)
Official Gene Symbol ZNF451 (GeneCards)
Number of variants in ZNF451 in this database 1 (view all the variants)
Full name zinc finger protein 451
Band 6p12.1
Other IDs Vega: OTTHUMG00000014916
OMIM: 615708
HGNC: HGNC:21091
Ensembl: ENSG00000112200
Other names COASTER, dJ417I1.1
Summary None

Individual #1

Individual ID 29217584.16 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Cockayne syndrome (view all the variants in this disease)
OMIM ID 216400

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;