| Variant ID | 22009 |
|---|---|
| Entrez Gene ID | 58526 |
| Gene | MID1IP1 (GeneCards) |
| Location | hg19 X:38822043-38822043
hg38 X:38962788-38962788 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000023.10:g.38822043 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) | 0.177329 (Deleterious) |
| FATHMM raw prediction score | 0.08144 (Tolerated) |
| Deleterious probability by DeFine | 0.0468 (Neutral) |
| Entrez Gene ID | 58526 (NCBI Gene) |
|---|---|
| Official Gene Symbol | MID1IP1 (GeneCards) |
| Number of variants in MID1IP1 in this database | 8 (view all the variants) |
| Full name | MID1 interacting protein 1 |
| Band | Xp11.4 |
| Other IDs | Vega: OTTHUMG00000024092 OMIM: 300961 HGNC: HGNC:20715 Ensembl: ENSG00000165175 |
| Other names | S14R, MIG12, THRSPL, G12-like, STRAIT11499 |
| 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; |