| Variant ID | 27265 |
|---|---|
| Entrez Gene ID | 101929222 |
| Gene | DISC1FP1 (GeneCards) |
| Location | hg19 11:91577527-91577527
hg38 11:91844361-91844361 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000011.9:g.91577527 C>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 |
|---|---|
| EIGEN score | 0.072 |
| CADD Raw score (version 1.3) | 0.060474 (Deleterious) |
| FATHMM raw prediction score | 0.15198 (Tolerated) |
| Deleterious probability by DeFine | 0.4729 (Neutral) |
| Entrez Gene ID | 101929222 (NCBI Gene) |
|---|---|
| Official Gene Symbol | DISC1FP1 (GeneCards) |
| Number of variants in DISC1FP1 in this database | 40 (view all the variants) |
| Full name | DISC1 fusion partner 1 |
| Band | 11q14.3 |
| Other IDs | HGNC: HGNC:33625 Ensembl: ENSG00000261645 |
| Other names | Boymaw |
| Summary | None |
| Individual ID | 29217587.02 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |