| Variant ID | 7513 |
|---|---|
| Entrez Gene ID | 1839 |
| Gene | HBEGF (GeneCards) |
| Location | hg19 5:139720439-139720439
hg38 5:140340854-140340854 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000005.9:g.139720439 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 | 180915260 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1164 |
| CADD Raw score (version 1.3) | 0.109173 (Deleterious) |
| FATHMM raw prediction score | 0.18702 (Tolerated) |
| Deleterious probability by DeFine | 0.5264 (Deleterious) |
| Entrez Gene ID | 1839 (NCBI Gene) |
|---|---|
| Official Gene Symbol | HBEGF (GeneCards) |
| Number of variants in HBEGF in this database | 1 (view all the variants) |
| Full name | heparin binding EGF like growth factor |
| Band | 5q31.3 |
| Other IDs | Vega: OTTHUMG00000129496 OMIM: 126150 HGNC: HGNC:3059 Ensembl: ENSG00000113070 |
| Other names | DTR, DTS, DTSF, HEGFL |
| Summary | None |
| 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; |