| Variant ID | 8984 |
|---|---|
| Entrez Gene ID | 10924 |
| Gene | SMPDL3A (GeneCards) |
| Location | hg19 6:123192099-123192099
hg38 6:122870954-122870954 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000006.11:g.123192099 A>G (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 | 171115067 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.3092 |
| CADD Raw score (version 1.3) | -0.055736 (Deleterious) |
| FATHMM raw prediction score | 0.06632 (Tolerated) |
| Deleterious probability by DeFine | 0.0759 (Neutral) |
| Entrez Gene ID | 10924 (NCBI Gene) |
|---|---|
| Official Gene Symbol | SMPDL3A (GeneCards) |
| Number of variants in SMPDL3A in this database | 7 (view all the variants) |
| Full name | sphingomyelin phosphodiesterase acid like 3A |
| Band | 6q22.31 |
| Other IDs | Vega: OTTHUMG00000015490 OMIM: 610728 HGNC: HGNC:17389 Ensembl: ENSG00000172594 |
| Other names | ASM3A, ASML3a, yR36GH4.1 |
| 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; |