Overview

Variant ID 4541
Entrez Gene ID 11069
Gene RAPGEF4 (GeneCards)
Location hg19 2:173793182-173793182
hg38 2:172928454-172928454
Disease Xeroderma Pigmentosum (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000002.11:g.173793182 T>C (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 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.1603
CADD Raw score (version 1.3) -0.004215 (Deleterious)
FATHMM raw prediction score 0.19326 (Tolerated)
Deleterious probability by DeFine 0.5482 (Deleterious)
Entrez Gene ID 11069 (NCBI Gene)
Official Gene Symbol RAPGEF4 (GeneCards)
Number of variants in RAPGEF4 in this database 3 (view all the variants)
Full name Rap guanine nucleotide exchange factor 4
Band 2q31.1
Other IDs Vega: OTTHUMG00000133677
OMIM: 606058
HGNC: HGNC:16626
Ensembl: ENSG00000091428
Other names EPAC, CGEF2, EPAC2, EPAC2, Nbla00496, CAMP-GEFII
Summary None

Individual #1

Individual ID 29217584.24 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Xeroderma Pigmentosum (view all the variants in this disease)
OMIM ID 278700

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;