Overview

Variant ID 9559
Entrez Gene ID 56995
Gene TULP4 (GeneCards)
Location hg19 6:158910400-158910400
hg38 6:158489368-158489368
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000006.11:g.158910400 A>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 -0.0869
CADD Raw score (version 1.3) -0.045433 (Deleterious)
FATHMM raw prediction score 0.1344 (Tolerated)
Deleterious probability by DeFine 0.5738 (Deleterious)
Entrez Gene ID 56995 (NCBI Gene)
Official Gene Symbol TULP4 (GeneCards)
Number of variants in TULP4 in this database 4 (view all the variants)
Full name tubby like protein 4
Band 6q25.3
Other IDs Vega: OTTHUMG00000015910
HGNC: HGNC:15530
Ensembl: ENSG00000130338
Other names TUSP
Summary None

Individual #1

Individual ID 29217584.11 (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;