| Variant ID | 6098 |
|---|---|
| Entrez Gene ID | 100507096 |
| Gene | GIMD1 (GeneCards) |
| Location | hg19 4:107776554-107776554
hg38 4:106855397-106855397 |
| Disease | Asymptomatic |
| Method | HiSeq 2000 |
| Mutation(HGVS format) | NC_000004.11:g.107776554 G>A (Genome Assembly: GRCh37) |
| 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 | 191154276 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1573 |
| CADD Raw score (version 1.3) | 0.410679 (Deleterious) |
| FATHMM raw prediction score | 0.18234 (Tolerated) |
| Deleterious probability by DeFine | 0.482 (Neutral) |
| Entrez Gene ID | 100507096 (NCBI Gene) |
|---|---|
| Official Gene Symbol | GIMD1 (GeneCards) |
| Number of variants in GIMD1 in this database | 10 (view all the variants) |
| Full name | GIMAP family P-loop NTPase domain containing 1 |
| Band | 4q24 |
| Other IDs | Vega: OTTHUMG00000161071 HGNC: HGNC:44141 Ensembl: ENSG00000250298 |
| Other names | None |
| Summary | None |
| Individual ID | 29217584.04 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| 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; |