| Variant ID | 16432 |
|---|---|
| Entrez Gene ID | 83857 |
| Gene | TMTC1 (GeneCards) |
| Location | hg19 12:29767516-29767516
hg38 12:29614583-29614583 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000012.11:g.29767516 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 | 133851895 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.1502 |
| CADD Raw score (version 1.3) | -0.037942 (Deleterious) |
| FATHMM raw prediction score | 0.08217 (Tolerated) |
| Deleterious probability by DeFine | 0.6079 (Deleterious) |
| Entrez Gene ID | 83857 (NCBI Gene) |
|---|---|
| Official Gene Symbol | TMTC1 (GeneCards) |
| Number of variants in TMTC1 in this database | 20 (view all the variants) |
| Full name | transmembrane and tetratricopeptide repeat containing 1 |
| Band | 12p11.22 |
| Other IDs | Vega: OTTHUMG00000169324 OMIM: 615855 HGNC: HGNC:24099 Ensembl: ENSG00000133687 |
| Other names | OLF, ARG99, TMTC1A |
| Summary | None |
| Individual ID | 29217584.09 (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; |