Variant ID | 23110 |
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Entrez Gene ID | 81491 |
Gene | GPR63 (GeneCards) |
Location | hg19 6:97277099-97277099
hg38 6:96829223-96829223 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000006.11:g.97277099 G>C (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 | 171115067 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3217 |
CADD Raw score (version 1.3) | -0.58486 (Deleterious) |
FATHMM raw prediction score | 0.08728 (Tolerated) |
Deleterious probability by DeFine | 0.1694 (Neutral) |
Entrez Gene ID | 81491 (NCBI Gene) |
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Official Gene Symbol | GPR63 (GeneCards) |
Number of variants in GPR63 in this database | 4 (view all the variants) |
Full name | G protein-coupled receptor 63 |
Band | 6q16.1 |
Other IDs | Vega: OTTHUMG00000015245 OMIM: 606915 HGNC: HGNC:13302 Ensembl: ENSG00000112218 |
Other names | PSP24B, PSP24(beta) |
Summary | This gene encodes a G protein-coupled receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Dec 2011] |
Individual ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
Journal | Science |
Publication date | 2018.02 |
Disease | Asymptomatic |
Number of cases | cases of unknown sex: 3; |