| Variant ID | 27517 |
|---|---|
| Entrez Gene ID | 100885789 |
| Gene | IFNG-AS1 (GeneCards) |
| Location | hg19 12:68510038-68510038
hg38 12:68116258-68116258 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000012.11:g.68510038 T>A (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 | 133851895 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.2786 |
| CADD Raw score (version 1.3) | 0.244645 (Deleterious) |
| FATHMM raw prediction score | 0.0893 (Tolerated) |
| Deleterious probability by DeFine | 0.0918 (Neutral) |
| Entrez Gene ID | 100885789 (NCBI Gene) |
|---|---|
| Official Gene Symbol | IFNG-AS1 (GeneCards) |
| Number of variants in IFNG-AS1 in this database | 5 (view all the variants) |
| Full name | IFNG antisense RNA 1 |
| Band | 12q15 |
| Other IDs | HGNC: HGNC:43910 Ensembl: ENSG00000255733 |
| Other names | NEST, Tmevpg1, GS1-410F4.2 |
| Summary | None |
| Individual ID | 29217587.02 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |