Variant ID | 28122 |
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Entrez Gene ID | 54386 |
Gene | TERF2IP (GeneCards) |
Location | hg19 16:76177533-76177533
hg38 16:76143635-76143635 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000016.9:g.76177533 C>A (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 | 90354753 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.29 |
CADD Raw score (version 1.3) | -0.050225 (Deleterious) |
FATHMM raw prediction score | 0.06176 (Tolerated) |
Deleterious probability by DeFine | 0.1945 (Neutral) |
Entrez Gene ID | 54386 (NCBI Gene) |
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Official Gene Symbol | TERF2IP (GeneCards) |
Number of variants in TERF2IP in this database | 5 (view all the variants) |
Full name | TERF2 interacting protein |
Band | 16q23.1 |
Other IDs | Vega: OTTHUMG00000177136 OMIM: 605061 HGNC: HGNC:19246 Ensembl: ENSG00000166848 |
Other names | RAP1, DRIP5 |
Summary | The gene encodes a protein that is part of a complex involved in telomere length regulation. Pseudogenes are present on chromosomes 5 and 22. [provided by RefSeq, Apr 2010] |
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 |