Overview

Variant ID 1995
Entrez Gene ID 23261
Gene CAMTA1 (GeneCards)
Location hg19 1:6916047-6916047
hg38 1:6855987-6855987
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000001.10:g.6916047 C>T (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 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1609
CADD Raw score (version 1.3) 0.138844 (Deleterious)
FATHMM raw prediction score 0.09725 (Tolerated)
Deleterious probability by DeFine 0.3068 (Neutral)
Entrez Gene ID 23261 (NCBI Gene)
Official Gene Symbol CAMTA1 (GeneCards)
Number of variants in CAMTA1 in this database 4 (view all the variants)
Full name calmodulin binding transcription activator 1
Band 1p36.31-p36.23
Other IDs Vega: OTTHUMG00000001212
OMIM: 611501
HGNC: HGNC:18806
Ensembl: ENSG00000171735
Other names CANPMR
Summary The protein encoded by this gene contains a CG1 DNA-binding domain, a transcription factor immunoglobulin domain, ankyrin repeats, and calmodulin-binding IQ motifs. The encoded protein is thought to be a transcription factor and may be a tumor suppressor. However, a translocation event is sometimes observed between this gene and the WWTR1 gene, with the resulting WWTR1-CAMTA1 oncoprotein leading to epithelioid hemangioendothelioma, a malignant vascular cancer. [provided by RefSeq, Mar 2017]

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;