| Variant ID | 21823 |
|---|---|
| Entrez Gene ID | 8911 |
| Gene | CACNA1I (GeneCards) |
| Location | hg19 22:40130860-40130860
hg38 22:39734855-39734855 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000022.10:g.40130860 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 | 51304566 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.3076 |
| CADD Raw score (version 1.3) | -0.103156 (Deleterious) |
| FATHMM raw prediction score | 0.07617 (Tolerated) |
| Deleterious probability by DeFine | 0.5233 (Deleterious) |
| Entrez Gene ID | 8911 (NCBI Gene) |
|---|---|
| Official Gene Symbol | CACNA1I (GeneCards) |
| Number of variants in CACNA1I in this database | 5 (view all the variants) |
| Full name | calcium voltage-gated channel subunit alpha1 I |
| Band | 22q13.1 |
| Other IDs | Vega: OTTHUMG00000151096 OMIM: 608230 HGNC: HGNC:1396 Ensembl: ENSG00000100346 |
| Other names | Cav3.3, ca(v)3.3 |
| Summary | This gene encodes the pore-forming alpha subunit of a voltage gated calcium channel. The encoded protein is a member of a subfamily of calcium channels referred to as is a low voltage-activated, T-type, calcium channel. The channel encoded by this protein is characterized by a slower activation and inactivation compared to other T-type calcium channels. This protein may be involved in calcium signaling in neurons. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011] |
| 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; |