Variant ID | 9277 |
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Entrez Gene ID | 56995 |
Gene | TULP4 (GeneCards) |
Location | hg19 6:158746655-158746655
hg38 6:158325623-158325623 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000006.11:g.158746655 G>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 | 171115067 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3713 |
CADD Raw score (version 1.3) | -0.208404 (Deleterious) |
FATHMM raw prediction score | 0.10568 (Tolerated) |
Deleterious probability by DeFine | 0.2582 (Neutral) |
Entrez Gene ID | 56995 (NCBI Gene) |
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Official Gene Symbol | TULP4 (GeneCards) |
Number of variants in TULP4 in this database | 4 (view all the variants) |
Full name | tubby like protein 4 |
Band | 6q25.3 |
Other IDs | Vega: OTTHUMG00000015910 HGNC: HGNC:15530 Ensembl: ENSG00000130338 |
Other names | TUSP |
Summary | None |
Individual ID | 29217584.08 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |