Variant ID | 30394 |
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Entrez Gene ID | 1788 |
Gene | DNMT3A (GeneCards) |
Location | hg19 2:25458608-25458608
hg38 2:25235739-25235739 |
Disease | Asymptomatic |
Method | smMIP |
Mutation(HGVS format) | NC_000002.11:g.25458608_25458608 del (Genome Assembly: hg19) |
Exon or Intron | Exon |
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Position in protein | 856 |
Amino acid changes in protein | E > NA |
Frameshift | fs |
Position in cDNA | 2565 |
Changes in cDNA | T > NA |
Indel | delT |
mRNA accession | NM_022552 |
mRNA length | NA |
Reference length | 243199373 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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Deleterious probability by DeFine | 0.955 (Deleterious) |
Entrez Gene ID | 1788 (NCBI Gene) |
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Official Gene Symbol | DNMT3A (GeneCards) |
Number of variants in DNMT3A in this database | 139 (view all the variants) |
Full name | DNA methyltransferase 3 alpha |
Band | 2p23.3 |
Other IDs | Vega: OTTHUMG00000094777 OMIM: 602769 HGNC: HGNC:2978 Ensembl: ENSG00000119772 |
Other names | TBRS, DNMT3A2, M.HsaIIIA |
Summary | CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase that is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes to the cytoplasm and nucleus and its expression is developmentally regulated. [provided by RefSeq, Mar 2016] |
Individual ID | 28669404.155 (view all the variants in this individual) |
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Pubmed ID | 28669404 |
Whose mosaic mutation | Normal |
Origin of mosaic mutation in patients | de novo |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 28669404 |
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Title | Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life |
Journal | American Journal of Human Genetics |
Publication date | 2017.07 |
Disease | Asymptomatic |
Number of cases | cases of unknown sex: 223; |