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Gene | DNMT3A |
Variant | L723fs |
Impact List | frameshift |
Protein Effect | loss of function |
Gene Variant Descriptions | DNMT3A L723fs results in a change in the amino acid sequence of the Dnmt3a protein beginning at aa 723 of 912, likely resulting in premature truncation of the functional protein (UniProt.org). L723fs confers a loss of function to the Dnmt3a protein as demonstrated by failure to dimerize with wild-type Dnmt3a and loss of methyltransferase activity in in vitro assays (PMID: 28872462). |
Associated Drug Resistance | |
Category Variants Paths |
DNMT3A mutant DNMT3A inact mut DNMT3A L723fs |
Transcript | NM_022552.5 |
gDNA | chr2:g.(25240646_25240647) |
cDNA | c.(2167_2166) |
Protein | p.L723fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_005264175 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_017003526.2 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_047443593.1 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_005264175.6 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_047443594.1 | chr2:g.(25234371_25234372) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_011532664 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_011532664.2 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
NM_175629 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
NM_175629.2 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_011532664.3 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
NM_022552.4 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_005264175.5 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_017003526.1 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
NM_022552.5 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
XM_017003526 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
NM_022552 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
NM_175629.2 | chr2:g.(25240646_25240647) | c.(2167_2166) | p.L723fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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