| Variant ID | 3373 |
|---|---|
| Entrez Gene ID | 80705 |
| Gene | TSGA10 (GeneCards) |
| Location | hg19 2:99749551-99749551
hg38 2:99133088-99133088 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000002.11:g.99749551 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 | 243199373 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.3196 |
| CADD Raw score (version 1.3) | -0.085667 (Deleterious) |
| FATHMM raw prediction score | 0.07567 (Tolerated) |
| Deleterious probability by DeFine | 0.0433 (Neutral) |
| Entrez Gene ID | 80705 (NCBI Gene) |
|---|---|
| Official Gene Symbol | TSGA10 (GeneCards) |
| Number of variants in TSGA10 in this database | 3 (view all the variants) |
| Full name | testis specific 10 |
| Band | 2q11.2 |
| Other IDs | Vega: OTTHUMG00000130637 OMIM: 607166 HGNC: HGNC:14927 Ensembl: ENSG00000135951 |
| Other names | CT79, CEP4L, SPGF26 |
| 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; |