Variant ID | 26688 |
---|---|
Entrez Gene ID | 10656 |
Gene | KHDRBS3 (GeneCards) |
Location | hg19 8:137988299-137988299
hg38 8:136976056-136976056 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000008.10:g.137988299 T>C (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 | 146364022 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
EIGEN score | -0.0059 |
CADD Raw score (version 1.3) | -0.13406 (Deleterious) |
FATHMM raw prediction score | 0.12518 (Tolerated) |
Deleterious probability by DeFine | 0.296 (Neutral) |
Entrez Gene ID | 10656 (NCBI Gene) |
---|---|
Official Gene Symbol | KHDRBS3 (GeneCards) |
Number of variants in KHDRBS3 in this database | 27 (view all the variants) |
Full name | KH RNA binding domain containing, signal transduction associated 3 |
Band | 8q24.23 |
Other IDs | Vega: OTTHUMG00000164164 OMIM: 610421 HGNC: HGNC:18117 Ensembl: ENSG00000131773 |
Other names | Etle, SALP, SLM2, SLM-2, TSTAR, T-STAR, etoile |
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 |