| Variant ID | 25679 |
|---|---|
| Entrez Gene ID | 56884 |
| Gene | FSTL5 (GeneCards) |
| Location | hg19 4:163354498-163354498
hg38 4:162433346-162433346 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000004.11:g.163354498 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 | 191154276 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.8717 |
| CADD Raw score (version 1.3) | -0.839207 (Deleterious) |
| FATHMM raw prediction score | 0.03996 (Tolerated) |
| Deleterious probability by DeFine | 0.1924 (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 |
| Individual ID | 29217587.03 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |