Variant ID | 13893 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 29217584.03 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |