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Gene | DNMT3A |
Variant | R635W |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | DNMT3A R635W lies within the SAM-dependent MTase C5-type domain of the Dnmt3a protein (UniProt.org). R635W (corresponding to R631W in mouse) confers a loss of function on Dnmt3a as indicated by loss of methylation activity, failure to be activated by Dnmt3L, failure to bind DNA in in vitro assays (PMID: 31861499), and reduced TDG activity in an in vitro assay (Blood (2016) 128 (22): 1076). |
Associated Drug Resistance | |
Category Variants Paths |
DNMT3A mutant DNMT3A inact mut DNMT3A R635W |
Transcript | NM_022552.5 |
gDNA | chr2:g.25243931G>A |
cDNA | c.1903C>T |
Protein | p.R635W |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_022552.4 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
NM_175629.2 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_017003526.1 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_005264175.6 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_005264175 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_017003526.2 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_011532664.3 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_011532664 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
NM_175629 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_011532664.2 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
NM_022552 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_005264175.5 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_017003526 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
NM_175629.2 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
XM_047443593.1 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
NM_022552.5 | chr2:g.25243931G>A | c.1903C>T | p.R635W | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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