Overview

Variant ID 942
Entrez Gene ID 8554
Gene PIAS1 (GeneCards)
Location hg19 15:68468935-68468935
hg38 15:68176597-68176597
Disease Human Skin Fibroblasts (view all the variants in this disease)
Method HiSeq 2500
Mutation(HGVS format) NC_000015.9:g.68468935 C>T (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 475
Amino acid changes in protein P > L
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 102531392

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.9025
CADD Raw score (version 1.3) 7.002344 (Deleterious)
FATHMM raw prediction score 0.98661 (Tolerated)
SIFT score 0.001 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 2.24 (Deleterious)
PROVEAN score -5.29 (Deleterious)
MetaSVM score -0.601 (Tolerated)
MetaLR score 0.263 (Tolerated)
MCAP score 0.02 (Tolerated)
FitCons score 0.707 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.93
PhyloP score based on multiple alignment of 100 vertebrates 7.239
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 20.351
Deleterious probability by iFish2 0.948 (Deleterious)
Deleterious probability by DeFine 0.9319 (Deleterious)
Entrez Gene ID 8554 (NCBI Gene)
Official Gene Symbol PIAS1 (GeneCards)
Number of variants in PIAS1 in this database 3 (view all the variants)
Full name protein inhibitor of activated STAT 1
Band 15q23
Other IDs Vega: OTTHUMG00000172645
OMIM: 603566
HGNC: HGNC:2752
Ensembl: ENSG00000033800
Other names GBP, ZMIZ3, DDXBP1, GU/RH-II
Summary This gene encodes a member of the protein inhibitor of activated STAT (PIAS) family. PIAS proteins function as SUMO E3 ligases and play important roles in many cellular processes by mediating the sumoylation of target proteins. This protein plays a central role as a transcriptional coregulator of numerous cellular pathways includign the STAT1 and nuclear factor kappaB pathways. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]

Individual #1

Individual ID 27788131.02 (view all the variants in this individual)
Pubmed ID 27788131
Whose mosaic mutation Normal  
Phenotype 1  
Disease Human Skin Fibroblasts (view all the variants in this disease)
OMIM ID 120353

Publication #1: 27788131

Pubmed ID 27788131
Title The Impact of Environmental and Endogenous Damage on Somatic Mutation Load in Human Skin Fibroblasts.
Journal PLoS Genetics
Publication date 2016.10
Disease Human Skin Fibroblasts
Population Caucasian
Number of cases Male cases: 2;