ClinVar Miner

List of variants in gene DNMT3A reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_022552.5(DNMT3A):c.1903C>T (p.Arg635Trp) rs144689354 0.00006
NM_022552.5(DNMT3A):c.2711C>T (p.Pro904Leu) rs149095705 0.00006
NM_022552.5(DNMT3A):c.1904G>A (p.Arg635Gln) rs751562376 0.00003
NM_022552.5(DNMT3A):c.1097G>A (p.Arg366His) rs767236033 0.00002
NM_022552.5(DNMT3A):c.1015-2A>G rs920946076 0.00001
NM_022552.5(DNMT3A):c.1907T>A (p.Val636Glu) rs929806900 0.00001
NM_022552.5(DNMT3A):c.2173+1G>A rs763716866 0.00001
NM_022552.5(DNMT3A):c.875T>C (p.Ile292Thr) rs777306476 0.00001
NM_022552.5(DNMT3A):c.130_131dup (p.Ala45fs) rs1553427894
NM_022552.5(DNMT3A):c.1443C>A (p.Tyr481Ter) rs145465364
NM_022552.5(DNMT3A):c.1450_1451dup (p.Gln485fs) rs1131691760
NM_022552.5(DNMT3A):c.1684T>C (p.Cys562Arg) rs1057520788
NM_022552.5(DNMT3A):c.1867dup (p.Tyr623fs) rs1553412022
NM_022552.5(DNMT3A):c.1906G>A (p.Val636Met) rs376550450
NM_022552.5(DNMT3A):c.1916T>C (p.Leu639Pro)
NM_022552.5(DNMT3A):c.1978T>C (p.Tyr660His) rs1674056899
NM_022552.5(DNMT3A):c.2051_2055del (p.Val684fs)
NM_022552.5(DNMT3A):c.2096G>A (p.Gly699Asp)
NM_022552.5(DNMT3A):c.2213T>G (p.Leu738Arg) rs745714537
NM_022552.5(DNMT3A):c.2252TCT[1] (p.Phe752del)
NM_022552.5(DNMT3A):c.2330C>A (p.Pro777His)
NM_022552.5(DNMT3A):c.241del (p.Asp81fs)
NM_022552.5(DNMT3A):c.2478+1G>T rs762213449
NM_022552.5(DNMT3A):c.2597+1G>T
NM_022552.5(DNMT3A):c.2644C>A (p.Arg882Ser) rs377577594
NM_022552.5(DNMT3A):c.2645G>A (p.Arg882His) rs147001633
NM_022552.5(DNMT3A):c.2657del (p.Gln886fs) rs1573291900
NM_022552.5(DNMT3A):c.448+1G>A rs2031953051
NM_022552.5(DNMT3A):c.700_709del (p.Gly234fs) rs1553414444
NM_022552.5(DNMT3A):c.997G>A (p.Asp333Asn) rs1573340335

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.