Variant ID | 27700 |
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Entrez Gene ID | 122011 |
Gene | CSNK1A1L (GeneCards) |
Location | hg19 13:37884402-37884402
hg38 13:37310265-37310265 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000013.10:g.37884402 T>G (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 | 115169878 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3337 |
CADD Raw score (version 1.3) | 0.020393 (Deleterious) |
FATHMM raw prediction score | 0.06844 (Tolerated) |
Deleterious probability by DeFine | 0.4037 (Neutral) |
Entrez Gene ID | 122011 (NCBI Gene) |
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Official Gene Symbol | CSNK1A1L (GeneCards) |
Number of variants in CSNK1A1L in this database | 10 (view all the variants) |
Full name | casein kinase 1 alpha 1 like |
Band | 13q13.3 |
Other IDs | Vega: OTTHUMG00000016748 HGNC: HGNC:20289 Ensembl: ENSG00000180138 |
Other names | CK1 |
Summary | None |
Individual ID | 29217587.02 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |