Overview

Variant ID 14601
Entrez Gene ID 80013
Gene FAM188A (GeneCards)
Location hg19 10:16422096-16422096
hg38 10:16380097-16380097
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000010.10:g.16422096 C>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 135534747

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.2153
CADD Raw score (version 1.3) 0.134185 (Deleterious)
FATHMM raw prediction score 0.17745 (Tolerated)
Deleterious probability by DeFine 0.4457 (Neutral)
Entrez Gene ID 80013 (NCBI Gene)
Official Gene Symbol FAM188A (GeneCards)
Number of variants in MINDY3 in this database 15 (view all the variants)
Full name MINDY lysine 48 deubiquitinase 3
Band 10p13
Other IDs Vega: OTTHUMG00000017734
OMIM: 611649
HGNC: HGNC:23578
Ensembl: ENSG00000148481
Other names CARP, DERP5, my042, MST126, FAM188A, MSTP126, C10orf97
Summary The protein encoded by this gene contains a caspase-associated recruitment domain and may function in apoptosis. It has been identified as a tumor suppressor in lung and gastric cancers, and a polymorphism in the gene may be associated with gastric cancer risk. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]

Individual #1

Individual ID 29217584.15 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;