| Variant ID | 17470 |
|---|---|
| Entrez Gene ID | 121952 |
| Gene | METTL21EP (GeneCards) |
| Location | hg19 13:103599741-103599741
hg38 13:102947391-102947391 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000013.10:g.103599741 T>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 | 115169878 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1978 |
| CADD Raw score (version 1.3) | 0.64399 (Deleterious) |
| FATHMM raw prediction score | 0.63893 (Tolerated) |
| Deleterious probability by DeFine | 0.4982 (Neutral) |
| Entrez Gene ID | 121952 (NCBI Gene) |
|---|---|
| Official Gene Symbol | METTL21EP (GeneCards) |
| Number of variants in METTL21EP in this database | 2 (view all the variants) |
| Full name | methyltransferase like 21E, pseudogene |
| Band | 13q33.1 |
| Other IDs | HGNC: HGNC:41948 Ensembl: ENSG00000250878 |
| Other names | METTL21CP1 |
| Summary | None |
| Individual ID | 29217584.10 (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; |