| Variant ID | 22828 |
|---|---|
| Entrez Gene ID | 63899 |
| Gene | NSUN3 (GeneCards) |
| Location | hg19 3:94155262-94155262
hg38 3:94436418-94436418 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000003.11:g.94155262 T>C (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 | 198022430 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 1.0565 |
| CADD Raw score (version 1.3) | 1.755737 (Deleterious) |
| FATHMM raw prediction score | 0.94418 (Tolerated) |
| Deleterious probability by DeFine | 0.7837 (Deleterious) |
| Entrez Gene ID | 63899 (NCBI Gene) |
|---|---|
| Official Gene Symbol | NSUN3 (GeneCards) |
| Number of variants in NSUN3 in this database | 10 (view all the variants) |
| Full name | NOP2/Sun RNA methyltransferase family member 3 |
| Band | 3q11.2 |
| Other IDs | Vega: OTTHUMG00000159025 OMIM: 617491 HGNC: HGNC:26208 Ensembl: ENSG00000178694 |
| Other names | MST077, MSTP077 |
| Summary | None |
| Individual ID | 29217587.01 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| Pubmed ID | 29217587 |
|---|---|
| Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
| Journal | Science |
| Publication date | 2018.02 |
| Disease | Asymptomatic |
| Number of cases | cases of unknown sex: 3; |