Variant ID | 952 |
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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) |
Exon or Intron | Exon |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 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; |