Overview

Variant ID 28321
Entrez Gene ID 10594
Gene PRPF8 (GeneCards)
Location hg19 17:1559246-1559246
hg38 17:1655952-1655952
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000017.10:g.1559246 A>G (Genome Assembly: GRCh37)

Other information

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 81195210

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.016
EIGEN score -0.3299
CADD Raw score (version 1.3) 0.229155 (Deleterious)
FATHMM raw prediction score 0.63362 (Tolerated)
Deleterious probability by DeFine 0.1301 (Neutral)
Entrez Gene ID 10594 (NCBI Gene)
Official Gene Symbol PRPF8 (GeneCards)
Number of variants in PRPF8 in this database 2 (view all the variants)
Full name pre-mRNA processing factor 8
Band 17p13.3
Other IDs Vega: OTTHUMG00000090553
OMIM: 607300
HGNC: HGNC:17340
Ensembl: ENSG00000174231
Other names PRP8, RP13, HPRP8, PRPC8, SNRNP220
Summary Pre-mRNA splicing occurs in 2 sequential transesterification steps. The protein encoded by this gene is a component of both U2- and U12-dependent spliceosomes, and found to be essential for the catalytic step II in pre-mRNA splicing process. It contains several WD repeats, which function in protein-protein interactions. This protein has a sequence similarity to yeast Prp8 protein. This gene is a candidate gene for autosomal dominant retinitis pigmentosa. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.03 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID