| Variant ID | 22373 |
|---|---|
| Entrez Gene ID | 80316 |
| Gene | PPP1R2P9 (GeneCards) |
| Location | hg19 X:42760273-42760273
hg38 X:42901024-42901024 |
| Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000023.10:g.42760273 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 | 155270560 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| CADD Raw score (version 1.3) | 1.361539 (Deleterious) |
| FATHMM raw prediction score | 0.14221 (Tolerated) |
| Deleterious probability by DeFine | 0.6462 (Deleterious) |
| Entrez Gene ID | 80316 (NCBI Gene) |
|---|---|
| Official Gene Symbol | PPP1R2P9 (GeneCards) |
| Number of variants in PPP1R2C in this database | 3 (view all the variants) |
| Full name | PPP1R2C family member C |
| Band | Xp11.3 |
| Other IDs | Vega: OTTHUMG00000021382 HGNC: HGNC:16324 Ensembl: ENSG00000102055 |
| Other names | I-4, PPP1R2P9 |
| Summary | None |
| Individual ID | 29217584.23 (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; |