Variant ID | 28402 |
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Entrez Gene ID | 64693 |
Gene | CTAGE1 (GeneCards) |
Location | hg19 18:20186770-20186770
hg38 18:22606807-22606807 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000018.9:g.20186770 C>T (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 | 78077248 |
MAF in gnomAD genome (version 2.0.1) | 0.0000323 |
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EIGEN score | -0.2069 |
CADD Raw score (version 1.3) | 0.453091 (Deleterious) |
FATHMM raw prediction score | 0.09921 (Tolerated) |
Deleterious probability by DeFine | 0.721 (Deleterious) |
Entrez Gene ID | 64693 (NCBI Gene) |
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Official Gene Symbol | CTAGE1 (GeneCards) |
Number of variants in CTAGE1 in this database | 5 (view all the variants) |
Full name | cutaneous T cell lymphoma-associated antigen 1 |
Band | 18q11.2 |
Other IDs | Vega: OTTHUMG00000165867 OMIM: 608856 HGNC: HGNC:24346 Ensembl: ENSG00000212710 |
Other names | CTAGE, CT21.1, CT21.2, CTAGE-1, CTAGE-2 |
Summary | None |
Individual ID | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |