| Variant ID | 29905 |
|---|---|
| Entrez Gene ID | 124535 |
| Gene | HSF5 (GeneCards) |
| Location | hg19 17:56536222-56536222
hg38 17:58458861-58458861 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | NextSeq500 |
| Mutation(HGVS format) | NC_000017.10:g.56536222 C>T (Genome Assembly: hg19) |
| Exon or Intron | Exon |
|---|---|
| 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 | 81195210 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1433 |
| CADD Raw score (version 1.3) | 4.680949 (Deleterious) |
| FATHMM raw prediction score | 0.6882 (Tolerated) |
| SIFT score | 0.061 (Tolerated) |
| LRT score | 0 (Deleterious) |
| MutationTaster score | 0.936 (Deleterious) |
| MutatioinAssessor score | 0.805 (Tolerated) |
| PROVEAN score | -1.17 (Tolerated) |
| MetaSVM score | -0.524 (Tolerated) |
| MetaLR score | 0.24 (Tolerated) |
| MCAP score | 0.035 (Deleterious) |
| FitCons score | 0.554 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | 4.79 |
| PhyloP score based on multiple alignment of 100 vertebrates | 1.632 |
| PhastCons score based on multiple alignment of 100 vertebrates | 1 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 14.12 |
| Deleterious probability by iFish2 | 0.1291 (Neutral) |
| Deleterious probability by DeFine | 0.8976 (Deleterious) |
| Entrez Gene ID | 124535 (NCBI Gene) |
|---|---|
| Official Gene Symbol | HSF5 (GeneCards) |
| Number of variants in HSF5 in this database | 4 (view all the variants) |
| Full name | heat shock transcription factor 5 |
| Band | 17q22 |
| Other IDs | Vega: OTTHUMG00000179078 HGNC: HGNC:26862 Ensembl: ENSG00000176160 |
| Other names | HSF5, HSTF5 |
| Summary | None |
| Individual ID | 28867142.20 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 28867142 |
| Whose mosaic mutation | Male Patient |
| Origin of mosaic mutation in patients | de novo |
| Phenotype | 3 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| OMIM ID | 209850 |
| Pubmed ID | 28867142 |
|---|---|
| Title | Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder |
| Journal | American Journal of Human Genetics |
| Publication date | 2017.08 |
| Disease | Autism Spectrum Disorders |
| Incidence | 0.01 |
| Number of cases | cases of unknown sex: 247; |