| Variant ID | 15018 |
|---|---|
| Entrez Gene ID | 120114 |
| Gene | FAT3 (GeneCards) |
| Location | hg19 11:92117149-92117149
hg38 11:92383983-92383983 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000011.9:g.92117149 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 | 135006516 |
| MAF in gnomAD genome (version 2.0.1) | 0.0147 |
|---|---|
| SNP ID (dbSNP ID version 137) | rs73548420 |
| EIGEN score | 0.5258 |
| CADD Raw score (version 1.3) | 0.761361 (Deleterious) |
| FATHMM raw prediction score | 0.18684 (Tolerated) |
| Deleterious probability by DeFine | 0.6636 (Deleterious) |
| Entrez Gene ID | 120114 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FAT3 (GeneCards) |
| Number of variants in FAT3 in this database | 6 (view all the variants) |
| Full name | FAT atypical cadherin 3 |
| Band | 11q14.3 |
| Other IDs | Vega: OTTHUMG00000154468 OMIM: 612483 HGNC: HGNC:23112 Ensembl: ENSG00000165323 |
| Other names | hFat3, CDHF15, CDHR10 |
| Summary | None |
| Individual ID | 29217584.03 (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; |