Variant ID | 26686 |
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Entrez Gene ID | 56169 |
Gene | GSDMC (GeneCards) |
Location | hg19 8:130807942-130807942
hg38 8:129795696-129795696 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000008.10:g.130807942 T>G (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 | 146364022 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1302 |
CADD Raw score (version 1.3) | 0.689069 (Deleterious) |
FATHMM raw prediction score | 0.17725 (Tolerated) |
Deleterious probability by DeFine | 0.0544 (Neutral) |
Entrez Gene ID | 56169 (NCBI Gene) |
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Official Gene Symbol | GSDMC (GeneCards) |
Number of variants in GSDMC in this database | 6 (view all the variants) |
Full name | gasdermin C |
Band | 8q24.21 |
Other IDs | Vega: OTTHUMG00000164851 OMIM: 608384 HGNC: HGNC:7151 Ensembl: ENSG00000147697 |
Other names | MLZE |
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 |