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Gene | DNMT3A |
Variant | P569_A574del |
Impact List | deletion |
Protein Effect | unknown |
Gene Variant Descriptions | DNMT3A P569_A574del results in the deletion of six amino acids in the ADD domain of the Dnmt3a protein from amino acids 569 to 574 (UniProt.org). P569_A574del has not been characterized in the scientific literature and therefore, its effect on Dnmt3a protein function is unknown (PubMed, Oct 2024). |
Associated Drug Resistance | |
Category Variants Paths |
DNMT3A mutant DNMT3A P569_A574del |
Transcript | NM_022552.5 |
gDNA | chr2:g.25244284_25244301del18 |
cDNA | c.1705_1722del18 |
Protein | p.P569_A574delPGAAQA |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_175629 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
NM_175629.2 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
NM_022552.4 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
XM_005264175.6 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574delPGAAQA | RefSeq | GRCh38/hg38 |
XM_011532664.2 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
XM_017003526.1 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
XM_047443598.1 | chr2:g.25239148_25239165del18 | c.1706_1723del18 | p.R569_N574delRYFWGN | RefSeq | GRCh38/hg38 |
NM_001320893.1 | chr2:g.25240448_25240654del207 | c.1706_1723del207 | p.K569_G574delKGLYEG | RefSeq | GRCh38/hg38 |
NM_153759.3 | chr2:g.25240336_25240353del18 | c.1705_1722del18 | p.V569_V574delVVAMGV | RefSeq | GRCh38/hg38 |
XM_047443594.1 | chr2:g.25240423_25240440del18 | c.1705_1722del18 | p.R569_F574delRLFFEF | RefSeq | GRCh38/hg38 |
NM_001375819.1 | chr2:g.25239148_25239165del18 | c.1706_1723del18 | p.R569_N574delRYFWGN | RefSeq | GRCh38/hg38 |
XM_011532666.3 | chr2:g.25240374_25240391del18 | c.1705_1722del18 | p.E569_P574delEGDDRP | RefSeq | GRCh38/hg38 |
XM_047443597.1 | chr2:g.25239148_25239165del18 | c.1706_1723del18 | p.R569_N574delRYFWGN | RefSeq | GRCh38/hg38 |
XM_047443593.1 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574delPGAAQA | RefSeq | GRCh38/hg38 |
XM_011532664 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
NM_022552.5 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574delPGAAQA | RefSeq | GRCh38/hg38 |
XM_017003527.2 | chr2:g.25239148_25239165del18 | c.1706_1723del18 | p.R569_N574delRYFWGN | RefSeq | GRCh38/hg38 |
XM_047443592.1 | chr2:g.25241625_25241642del18 | c.1705_1722del18 | p.D569_G574delDSITVG | RefSeq | GRCh38/hg38 |
XM_005264175.5 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
XM_005264175 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
XM_011532667.4 | chr2:g.25239148_25239165del18 | c.1706_1723del18 | p.R569_N574delRYFWGN | RefSeq | GRCh38/hg38 |
XM_011532662.3 | chr2:g.25243965_25243982del18 | c.1705_1722del18 | p.D569_Y574delDPPKVY | RefSeq | GRCh38/hg38 |
NM_175629.2 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574delPGAAQA | RefSeq | GRCh38/hg38 |
XM_017003526.2 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574delPGAAQA | RefSeq | GRCh38/hg38 |
NM_022552 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
XM_017003526 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574del | RefSeq | GRCh38/hg38 |
XM_047443596.1 | chr2:g.25239148_25239165del18 | c.1706_1723del18 | p.R569_N574delRYFWGN | RefSeq | GRCh38/hg38 |
XM_011532664.3 | chr2:g.25244284_25244301del18 | c.1705_1722del18 | p.P569_A574delPGAAQA | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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