| Variant ID | 28832 |
|---|---|
| Entrez Gene ID | 170062 |
| Gene | FAM47B (GeneCards) |
| Location | hg19 X:35770880-35770880
hg38 X:35752763-35752763 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000023.10:g.35770880 G>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 | 155270560 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| CADD Raw score (version 1.3) | -0.244999 (Deleterious) |
| FATHMM raw prediction score | 0.07615 (Tolerated) |
| Deleterious probability by DeFine | 0.3552 (Neutral) |
| Entrez Gene ID | 170062 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FAM47B (GeneCards) |
| Number of variants in FAM47B in this database | 9 (view all the variants) |
| Full name | family with sequence similarity 47 member B |
| Band | Xp21.1 |
| Other IDs | Vega: OTTHUMG00000021345 HGNC: HGNC:26659 Ensembl: ENSG00000189132 |
| Other names | None |
| 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 |