Variant ID | 7777 |
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Entrez Gene ID | 5924 |
Gene | RASGRF2 (GeneCards) |
Location | hg19 5:80302505-80302505
hg38 5:81006686-81006686 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000005.9:g.80302505 C>T (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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0.0002 |
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EIGEN score | -0.4039 |
CADD Raw score (version 1.3) | -0.252587 (Deleterious) |
FATHMM raw prediction score | 0.07287 (Tolerated) |
Deleterious probability by DeFine | 0.3049 (Neutral) |
Entrez Gene ID | 5924 (NCBI Gene) |
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Official Gene Symbol | RASGRF2 (GeneCards) |
Number of variants in RASGRF2 in this database | 5 (view all the variants) |
Full name | Ras protein specific guanine nucleotide releasing factor 2 |
Band | 5q14.1 |
Other IDs | Vega: OTTHUMG00000119015 OMIM: 606614 HGNC: HGNC:9876 Ensembl: ENSG00000113319 |
Other names | GRF2, RAS-GRF2 |
Summary | RAS GTPases cycle between an inactive GDP-bound state and an active GTP-bound state. This gene encodes a calcium-regulated nucleotide exchange factor activating both RAS and RAS-related protein, RAC1, through the exchange of bound GDP for GTP, thereby, coordinating the signaling of distinct mitogen-activated protein kinase pathways. [provided by RefSeq, Oct 2011] |
Individual ID | 29217584.07 (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; |