Variant ID | 27563 |
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Entrez Gene ID | 92293 |
Gene | TMEM132C (GeneCards) |
Location | hg19 12:128960963-128960963
hg38 12:128476418-128476418 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000012.11:g.128960963 G>A (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 | 133851895 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.138 |
CADD Raw score (version 1.3) | -0.100764 (Deleterious) |
FATHMM raw prediction score | 0.10992 (Tolerated) |
Deleterious probability by DeFine | 0.6273 (Deleterious) |
Entrez Gene ID | 92293 (NCBI Gene) |
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Official Gene Symbol | TMEM132C (GeneCards) |
Number of variants in TMEM132C in this database | 5 (view all the variants) |
Full name | transmembrane protein 132C |
Band | 12q24.32-q24.33 |
Other IDs | Vega: OTTHUMG00000163736 HGNC: HGNC:25436 Ensembl: ENSG00000181234 |
Other names | PPP1R152 |
Summary | None |
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 |