| Variant ID | 29251 |
|---|---|
| Entrez Gene ID | 114899 |
| Gene | C1QTNF3 (GeneCards) |
| Location | hg19 5:34028963-34028963
hg38 5:34028858-34028858 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | PASM |
| Mutation(HGVS format) | NC_000005.9:g.34028963 G>A (Genome Assembly: GRCh37) |
| 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 | 180915260 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.7409 |
| CADD Raw score (version 1.3) | 6.247433 (Deleterious) |
| FATHMM raw prediction score | 0.99135 (Tolerated) |
| SIFT score | 0.013 (Deleterious) |
| MutationTaster score | 1 (Deleterious) |
| MutatioinAssessor score | 2.825 (Deleterious) |
| PROVEAN score | -3.12 (Deleterious) |
| MetaSVM score | -0.047 (Tolerated) |
| MetaLR score | 0.534 (Deleterious) |
| MCAP score | 0.071 (Deleterious) |
| FitCons score | 0.554 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | 5.56 |
| PhyloP score based on multiple alignment of 100 vertebrates | 7.162 |
| PhastCons score based on multiple alignment of 100 vertebrates | 1 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 19.891 |
| Deleterious probability by iFish2 | 0.9493 (Deleterious) |
| Deleterious probability by DeFine | 0.9437 (Deleterious) |
| Entrez Gene ID | 114899 (NCBI Gene) |
|---|---|
| Official Gene Symbol | C1QTNF3 (GeneCards) |
| Number of variants in C1QTNF3 in this database | 2 (view all the variants) |
| Full name | C1q and TNF related 3 |
| Band | 5p13.2 |
| Other IDs | Vega: OTTHUMG00000090735 OMIM: 612045 HGNC: HGNC:14326 Ensembl: ENSG00000082196 |
| Other names | CORS, CORCS, CTRP3, CORS26, C1ATNF3, CORS-26 |
| Summary | None |
| Individual ID | 28503910.128 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 28503910 |
| Whose mosaic mutation | Patient |
| Phenotype | 3 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| OMIM ID | 209850 |
| Pubmed ID | 28503910 |
|---|---|
| Title | Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations |
| Journal | Human Mutation |
| Publication date | 2017.05 |
| Disease | Autism Spectrum Disorders |
| Incidence | 0.01 |
| Number of cases | cases of unknown sex: 215; |