| Variant ID | 6586 |
|---|---|
| Entrez Gene ID | 56884 |
| Gene | FSTL5 (GeneCards) |
| Location | hg19 4:162653713-162653713
hg38 4:161732561-161732561 |
| Disease | |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000004.11:g.162653713 C>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 | 191154276 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.6673 |
| CADD Raw score (version 1.3) | -0.556357 (Deleterious) |
| FATHMM raw prediction score | 0.03581 (Tolerated) |
| Deleterious probability by DeFine | 0.1861 (Neutral) |
| Entrez Gene ID | 56884 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FSTL5 (GeneCards) |
| Number of variants in FSTL5 in this database | 22 (view all the variants) |
| Full name | follistatin like 5 |
| Band | 4q32.2 |
| Other IDs | Vega: OTTHUMG00000161397 HGNC: HGNC:21386 Ensembl: ENSG00000168843 |
| Other names | None |
| Summary | None |
| 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; |