ClinVar Miner

Submissions for variant NM_022552.4(DNMT3A):c.2644C>T (p.Arg882Cys) (rs377577594)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000429128 SCV000503763 pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439787 SCV000503764 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422474 SCV000503765 likely pathogenic Myelodysplastic syndrome 2016-05-31 no assertion criteria provided literature only
OMIM RCV000590987 SCV000700194 pathogenic Tatton-Brown-rahman syndrome 2018-05-08 no assertion criteria provided literature only
OMIM RCV000429128 SCV000700195 pathogenic Acute myeloid leukemia 2018-05-08 no assertion criteria provided literature only

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.