Variant ID | 25728 |
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Entrez Gene ID | 5161 |
Gene | PDHA2 (GeneCards) |
Location | hg19 4:97742284-97742284
hg38 4:96821133-96821133 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000004.11:g.97742284 T>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 | 191154276 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1635 |
CADD Raw score (version 1.3) | -0.28837 (Deleterious) |
FATHMM raw prediction score | 0.11978 (Tolerated) |
Deleterious probability by DeFine | 0.4296 (Neutral) |
Entrez Gene ID | 5161 (NCBI Gene) |
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Official Gene Symbol | PDHA2 (GeneCards) |
Number of variants in PDHA2 in this database | 23 (view all the variants) |
Full name | pyruvate dehydrogenase E1 alpha 2 subunit |
Band | 4q22.3 |
Other IDs | Vega: OTTHUMG00000130990 OMIM: 179061 HGNC: HGNC:8807 Ensembl: ENSG00000163114 |
Other names | PDHAL |
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 |