Variant ID | 1047 |
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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) |
Exon or Intron | Exon |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 27788131.02 (view all the variants in this individual) |
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Pubmed ID | 27788131 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Human Skin Fibroblasts (view all the variants in this disease) |
OMIM ID | 120353 |
Pubmed ID | 27788131 |
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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; |