Variant ID | 27568 |
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Entrez Gene ID | 121536 |
Gene | AEBP2 (GeneCards) |
Location | hg19 12:19932465-19932465
hg38 12:19779531-19779531 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000012.11:g.19932465 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 | 133851895 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.2342 |
CADD Raw score (version 1.3) | -0.087546 (Deleterious) |
FATHMM raw prediction score | 0.09099 (Tolerated) |
Deleterious probability by DeFine | 0.1841 (Neutral) |
Entrez Gene ID | 121536 (NCBI Gene) |
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Official Gene Symbol | AEBP2 (GeneCards) |
Number of variants in AEBP2 in this database | 13 (view all the variants) |
Full name | AE binding protein 2 |
Band | 12p12.3 |
Other IDs | Vega: OTTHUMG00000168906 OMIM: 617934 HGNC: HGNC:24051 Ensembl: ENSG00000139154 |
Other names | None |
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 |