Overview

Variant ID 945
Entrez Gene ID 5198
Gene PFAS (GeneCards)
Location hg19 17:8158388-8158388
hg38 17:8255070-8255070
Disease Human Skin Fibroblasts (view all the variants in this disease)
Method HiSeq 2500
Mutation(HGVS format) NC_000017.10:g.8158388 T>A (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 108
Amino acid changes in protein C > S
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
EIGEN score 0.4829
CADD Raw score (version 1.3) 4.712694 (Deleterious)
FATHMM raw prediction score 0.9923 (Tolerated)
SIFT score 0.05 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 2.81 (Deleterious)
PROVEAN score -8.1 (Deleterious)
MetaSVM score -0.845 (Tolerated)
MetaLR score 0.142 (Tolerated)
MCAP score 0.051 (Deleterious)
FitCons score 0.707 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.2
PhyloP score based on multiple alignment of 100 vertebrates 7.058
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 13.303
Deleterious probability by iFish2 0.5125 (Deleterious)
Deleterious probability by DeFine 0.9655 (Deleterious)
Entrez Gene ID 5198 (NCBI Gene)
Official Gene Symbol PFAS (GeneCards)
Number of variants in PFAS in this database 1 (view all the variants)
Full name phosphoribosylformylglycinamidine synthase
Band 17p13.1
Other IDs Vega: OTTHUMG00000108188
OMIM: 602133
HGNC: HGNC:8863
Ensembl: ENSG00000178921
Other names PURL, FGAMS, GATD8, FGARAT, FGAR-AT
Summary Purines are necessary for many cellular processes, including DNA replication, transcription, and energy metabolism. Ten enzymatic steps are required to synthesize inosine monophosphate (IMP) in the de novo pathway of purine biosynthesis. The enzyme encoded by this gene catalyzes the fourth step of IMP biosynthesis. [provided by RefSeq, Jul 2008]

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;