Variant ID | 27123 |
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Entrez Gene ID | 80013 |
Gene | FAM188A (GeneCards) |
Location | hg19 10:16232515-16232515
hg38 10:16190516-16190516 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000010.10:g.16232515 G>T (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3253 |
CADD Raw score (version 1.3) | -0.162619 (Deleterious) |
FATHMM raw prediction score | 0.08503 (Tolerated) |
Deleterious probability by DeFine | 0.049 (Neutral) |
Entrez Gene ID | 80013 (NCBI Gene) |
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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 ID | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |