Overview

Variant ID 13893
Entrez Gene ID 6251
Gene RSU1 (GeneCards)
Location hg19 10:16792325-16792325
hg38 10:16750326-16750326
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000010.10:g.16792325 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 135534747

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0215
CADD Raw score (version 1.3) 0.186642 (Deleterious)
FATHMM raw prediction score 0.13401 (Tolerated)
Deleterious probability by DeFine 0.341 (Neutral)
Entrez Gene ID 6251 (NCBI Gene)
Official Gene Symbol RSU1 (GeneCards)
Number of variants in RSU1 in this database 3 (view all the variants)
Full name Ras suppressor protein 1
Band 10p13
Other IDs Vega: OTTHUMG00000017740
OMIM: 179555
HGNC: HGNC:10464
Ensembl: ENSG00000148484
Other names RSP-1
Summary This gene encodes a protein that is involved in the Ras signal transduction pathway, growth inhibition, and nerve-growth factor induced differentiation processes, as determined in mouse and human cell line studies. In mouse, the encoded protein was initially isolated based on its ability to inhibit v-Ras transformation. Multiple alternatively spliced transcript variants for this gene have been reported; one of these variants was found only in glioma tumors. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.03 (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;