ClinVar Miner

List of variants in gene EHMT1 reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
Download table as spreadsheet
HGVS dbSNP
NM_024757.5(EHMT1):c.102C>T (p.Ala34=) rs202208554
NM_024757.5(EHMT1):c.1133C>T (p.Ser378Phe) rs780462689
NM_024757.5(EHMT1):c.1176C>T (p.Asp392=) rs373083497
NM_024757.5(EHMT1):c.128_129delinsGT (p.Ala43Gly) rs386739686
NM_024757.5(EHMT1):c.21+10G>C rs1040872282
NM_024757.5(EHMT1):c.2181C>T (p.Leu727=) rs377163037
NM_024757.5(EHMT1):c.2280C>T (p.Asp760=) rs372779658
NM_024757.5(EHMT1):c.240C>T (p.Asn80=) rs752561133
NM_024757.5(EHMT1):c.2595C>T (p.Asp865=) rs780742937
NM_024757.5(EHMT1):c.2616A>G (p.Gly872=) rs779277999
NM_024757.5(EHMT1):c.271A>T (p.Ile91Leu) rs144949902
NM_024757.5(EHMT1):c.276G>A (p.Ala92=) rs376810828
NM_024757.5(EHMT1):c.2799C>T (p.His933=) rs573774002
NM_024757.5(EHMT1):c.2808C>T (p.Asn936=) rs553009659
NM_024757.5(EHMT1):c.2865C>T (p.Val955=) rs749354858
NM_024757.5(EHMT1):c.2922G>A (p.Thr974=) rs748716122
NM_024757.5(EHMT1):c.2937G>A (p.Ala979=) rs564664932
NM_024757.5(EHMT1):c.2994G>C (p.Ser998=) rs778296046
NM_024757.5(EHMT1):c.3011G>A (p.Ser1004Asn) rs138283222
NM_024757.5(EHMT1):c.3059G>A (p.Arg1020His) rs376628665
NM_024757.5(EHMT1):c.3123C>G (p.Val1041=) rs141527497
NM_024757.5(EHMT1):c.3181-8C>T rs1554896993
NM_024757.5(EHMT1):c.3183C>T (p.Tyr1061=) rs1554896995
NM_024757.5(EHMT1):c.3321C>T (p.His1107=) rs781426172
NM_024757.5(EHMT1):c.33G>A (p.Ala11=) rs754740754
NM_024757.5(EHMT1):c.342T>C (p.Phe114=) rs1554846429
NM_024757.5(EHMT1):c.3522C>T (p.Leu1174=) rs748135858
NM_024757.5(EHMT1):c.3716+4C>T rs375271697
NM_024757.5(EHMT1):c.3716+9C>T rs777993644
NM_024757.5(EHMT1):c.3726T>C (p.Tyr1242=) rs1160822224
NM_024757.5(EHMT1):c.3747C>T (p.Ile1249=) rs1554908854
NM_024757.5(EHMT1):c.3774C>T (p.Cys1258=) rs371136319
NM_024757.5(EHMT1):c.390G>T (p.Pro130=) rs144323841
NM_024757.5(EHMT1):c.438G>A (p.Ser146=) rs151008340
NM_024757.5(EHMT1):c.498C>T (p.Ser166=) rs146037252
NM_024757.5(EHMT1):c.576G>A (p.Pro192=) rs574514175
NM_024757.5(EHMT1):c.624G>A (p.Pro208=) rs759629407
NM_024757.5(EHMT1):c.737G>A (p.Arg246Gln) rs144871446
NM_024757.5(EHMT1):c.85+9G>A rs566701810
NM_024757.5(EHMT1):c.900T>C (p.Pro300=) rs1554858785

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.