Overview

Variant ID 952
Entrez Gene ID 128876
Gene FAM83C (GeneCards)
Location hg19 20:33876612-33876612
hg38 20:35288809-35288809
Disease Human Skin Fibroblasts (view all the variants in this disease)
Method HiSeq 2500
Mutation(HGVS format) NC_000020.10:g.33876612 G>A (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 221
Amino acid changes in protein L > L
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 63025520

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.9968
CADD Raw score (version 1.3) -0.183182 (Deleterious)
FATHMM raw prediction score 0.96638 (Tolerated)
Deleterious probability by DeFine 0.8434 (Deleterious)
Entrez Gene ID 128876 (NCBI Gene)
Official Gene Symbol FAM83C (GeneCards)
Number of variants in FAM83C in this database 1 (view all the variants)
Full name family with sequence similarity 83 member C
Band 20q11.22
Other IDs Vega: OTTHUMG00000032332
HGNC: HGNC:16121
Ensembl: ENSG00000125998
Other names C20orf128, dJ614O4.7
Summary This gene encodes a member of the family with sequence similarity 83 protein family. The encoded protein may be involved in regulating MAPK signaling in cancer cells. [provided by RefSeq, Mar 2017]

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;