| Variant ID | 14966 |
|---|---|
| Entrez Gene ID | 103695365 |
| Gene | LINC01435 (GeneCards) |
| Location | hg19 10:109770375-109770375
hg38 10:108010617-108010617 |
| Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000010.10:g.109770375 G>A (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 | 135534747 |
| MAF in gnomAD genome (version 2.0.1) | 0.00009687 |
|---|---|
| EIGEN score | -0.174 |
| CADD Raw score (version 1.3) | -0.167677 (Deleterious) |
| FATHMM raw prediction score | 0.04261 (Tolerated) |
| Deleterious probability by DeFine | 0.306 (Neutral) |
| Entrez Gene ID | 103695365 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC01435 (GeneCards) |
| Number of variants in LINC01435 in this database | 20 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 1435 |
| Band | 10q25.1 |
| Other IDs | HGNC: HGNC:50753 Ensembl: ENSG00000229981 |
| Other names | TCONS_00018040 |
| Summary | None |
| Individual ID | 29217584.24 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Female Patient |
| Phenotype | 3 |
| Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
| OMIM ID | 278700 |
| 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; |