| Variant ID | 25357 |
|---|---|
| Entrez Gene ID | 5067 |
| Gene | CNTN3 (GeneCards) |
| Location | hg19 3:74505150-74505150
hg38 3:74455999-74455999 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000003.11:g.74505150 A>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 | -0.1168 |
| CADD Raw score (version 1.3) | -0.24885 (Deleterious) |
| FATHMM raw prediction score | 0.10206 (Tolerated) |
| Deleterious probability by DeFine | 0.3395 (Neutral) |
| Entrez Gene ID | 5067 (NCBI Gene) |
|---|---|
| Official Gene Symbol | CNTN3 (GeneCards) |
| Number of variants in CNTN3 in this database | 12 (view all the variants) |
| Full name | contactin 3 |
| Band | 3p12.3 |
| Other IDs | Vega: OTTHUMG00000158813 OMIM: 601325 HGNC: HGNC:2173 Ensembl: ENSG00000113805 |
| Other names | PCS, PANG, BIG-1 |
| 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 |