| Variant ID | 24955 |
|---|---|
| Entrez Gene ID | 55137 |
| Gene | FIGN (GeneCards) |
| Location | hg19 2:165287665-165287665
hg38 2:164431155-164431155 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000002.11:g.165287665 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 | 243199373 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1208 |
| CADD Raw score (version 1.3) | 0.036813 (Deleterious) |
| FATHMM raw prediction score | 0.16019 (Tolerated) |
| Deleterious probability by DeFine | 0.7063 (Deleterious) |
| Entrez Gene ID | 55137 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FIGN (GeneCards) |
| Number of variants in FIGN in this database | 8 (view all the variants) |
| Full name | fidgetin, microtubule severing factor |
| Band | 2q24.3 |
| Other IDs | Vega: OTTHUMG00000074059 OMIM: 605295 HGNC: HGNC:13285 Ensembl: ENSG00000182263 |
| Other names | None |
| Summary | None |
| Individual ID | 29217587.03 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |