| Variant ID | 26991 |
|---|---|
| Entrez Gene ID | 54462 |
| Gene | CCSER2 (GeneCards) |
| Location | hg19 10:86334157-86334157
hg38 10:84574401-84574401 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000010.10:g.86334157 C>T (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 | 135534747 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1146 |
| CADD Raw score (version 1.3) | 0.391729 (Deleterious) |
| FATHMM raw prediction score | 0.10429 (Tolerated) |
| Deleterious probability by DeFine | 0.1919 (Neutral) |
| Entrez Gene ID | 54462 (NCBI Gene) |
|---|---|
| Official Gene Symbol | CCSER2 (GeneCards) |
| Number of variants in CCSER2 in this database | 16 (view all the variants) |
| Full name | coiled-coil serine rich protein 2 |
| Band | 10q23.1 |
| Other IDs | Vega: OTTHUMG00000018641 HGNC: HGNC:29197 Ensembl: ENSG00000107771 |
| Other names | Gcap14, FAM190B, KIAA1128, bA486O22.1 |
| 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 |