Overview

Variant ID 1047
Entrez Gene ID 56927
Gene GPR108 (GeneCards)
Location hg19 19:6735688-6735688
hg38 19:6735677-6735677
Disease Human Skin Fibroblasts (view all the variants in this disease)
Method HiSeq 2500
Mutation(HGVS format) NC_000019.9:g.6735688 G>A (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 107
Amino acid changes in protein Q > *
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 59128983

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.1626
CADD Raw score (version 1.3) 8.080249 (Deleterious)
FATHMM raw prediction score 0.52871 (Tolerated)
LRT score 0.161
MutationTaster score 1 (Deleterious)
FitCons score 0.733 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 0.756
PhyloP score based on multiple alignment of 100 vertebrates -0.053
PhastCons score based on multiple alignment of 100 vertebrates 0
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 1.674
Deleterious probability by DeFine 0.684 (Deleterious)
Entrez Gene ID 56927 (NCBI Gene)
Official Gene Symbol GPR108 (GeneCards)
Number of variants in GPR108 in this database 1 (view all the variants)
Full name G protein-coupled receptor 108
Band 19p13.3
Other IDs Vega: OTTHUMG00000170129
HGNC: HGNC:17829
Ensembl: ENSG00000125734
Other names LUSTR2
Summary None

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;