Overview

Variant ID 30462
Entrez Gene ID 7307
Gene U2AF1 (GeneCards)
Location hg19 21:44524456-44524456
hg38 21:43104346-43104346
Disease Asymptomatic
Method smMIP
Mutation(HGVS format) NC_000021.8:g.44524456 C>T (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 34
Amino acid changes in protein S > F
Position in cDNA 101
Changes in cDNA C > T
mRNA accession NM_006758
mRNA length NA
Reference length 48129895

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
Variant IDs in COSMIC (version 89) 1190367
Variant occurences in COSMIC 6(haematopoietic_and_lymphoid_tissue)|1(lung)
EIGEN score 1.0441
CADD Raw score (version 1.3) 6.668304 (Deleterious)
FATHMM raw prediction score 0.98322 (Tolerated)
SIFT score 0 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 3.875 (Deleterious)
PROVEAN score -5.64 (Deleterious)
MetaSVM score 0.082 (Deleterious)
MetaLR score 0.41 (Tolerated)
MCAP score 0.127 (Deleterious)
FitCons score 0.722 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.47
PhyloP score based on multiple alignment of 100 vertebrates 9.053
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 19.317
Deleterious probability by DeFine 0.9242 (Deleterious)
Entrez Gene ID 7307 (NCBI Gene)
Official Gene Symbol U2AF1 (GeneCards)
Number of variants in U2AF1 in this database 3 (view all the variants)
Full name U2 small nuclear RNA auxiliary factor 1
Band 21q22.3
Other IDs Vega: OTTHUMG00000086836
OMIM: 191317
HGNC: HGNC:12453
Ensembl: ENSG00000160201
Other names RN, FP793, U2AF35, U2AFBP, RNU2AF1
Summary This gene belongs to the splicing factor SR family of genes. U2 auxiliary factor, comprising a large and a small subunit, is a non-snRNP protein required for the binding of U2 snRNP to the pre-mRNA branch site. This gene encodes the small subunit which plays a critical role in both constitutive and enhancer-dependent RNA splicing by directly mediating interactions between the large subunit and proteins bound to the enhancers. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 28669404.223 (view all the variants in this individual)
Pubmed ID 28669404
Whose mosaic mutation Normal  
Origin of mosaic mutation in patients de novo
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 28669404

Pubmed ID 28669404
Title Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life
Journal American Journal of Human Genetics
Publication date 2017.07
Disease Asymptomatic
Number of cases cases of unknown sex: 223;