ClinVar Miner

List of variants in gene combination INMT, INMT-MINDY4

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006774.5(INMT):c.791G>C (p.Ter264Ser) rs61741736 0.02173
NM_006774.5(INMT):c.567G>A (p.Pro189=) rs10225477 0.01309
NM_006774.5(INMT):c.340G>A (p.Ala114Thr) rs76338133 0.01154
NM_006774.5(INMT):c.435G>A (p.Leu145=) rs115699009 0.00948
NM_006774.5(INMT):c.339C>T (p.Phe113=) rs116690173 0.00595
NM_006774.5(INMT):c.367C>T (p.Arg123Ter) rs6966017 0.00426
NM_006774.5(INMT):c.252C>T (p.Ser84=) rs141846285 0.00138
NM_006774.5(INMT):c.363-7T>A rs373009361 0.00058
NM_006774.5(INMT):c.605C>T (p.Pro202Leu) rs147878270 0.00027
NM_006774.5(INMT):c.262G>A (p.Asp88Asn) rs141658794 0.00019
NM_006774.5(INMT):c.421T>C (p.Cys141Arg) rs778230606 0.00007
NM_006774.5(INMT):c.127G>A (p.Glu43Lys) rs781216470 0.00006
NM_006774.5(INMT):c.625C>T (p.Arg209Cys) rs193920790 0.00006
NM_006774.5(INMT):c.624G>C (p.Lys208Asn) rs145461151 0.00005
NM_006774.5(INMT):c.7G>A (p.Gly3Ser) rs780546755 0.00004
NM_006774.5(INMT):c.230C>T (p.Ser77Phe) rs749098351 0.00002
NM_006774.5(INMT):c.370T>C (p.Trp124Arg) rs776872677 0.00002
NM_006774.5(INMT):c.530G>A (p.Arg177His) rs996421042 0.00002
NM_006774.5(INMT):c.598C>T (p.Arg200Trp) rs140032041 0.00002
NM_006774.5(INMT):c.106G>A (p.Glu36Lys) rs777797023 0.00001
NM_006774.5(INMT):c.274G>A (p.Glu92Lys) rs193108315 0.00001
NM_006774.5(INMT):c.409C>T (p.Arg137Trp) rs757254092 0.00001
NM_006774.5(INMT):c.502T>C (p.Cys168Arg) rs975439738 0.00001
NM_006774.5(INMT):c.143C>T (p.Thr48Ile)
NM_006774.5(INMT):c.197C>T (p.Pro66Leu)
NM_006774.5(INMT):c.304C>A (p.Pro102Thr) rs1302987530
NM_006774.5(INMT):c.363C>A (p.Ser121Arg) rs201848016
NM_006774.5(INMT):c.363C>T (p.Ser121=)
NM_006774.5(INMT):c.400G>A (p.Ala134Thr) rs1786209390
NM_006774.5(INMT):c.452C>T (p.Pro151Leu)
NM_006774.5(INMT):c.491T>C (p.Leu164Pro)
NM_006774.5(INMT):c.526T>A (p.Tyr176Asn)
NM_006774.5(INMT):c.53G>C (p.Arg18Thr)
NM_006774.5(INMT):c.572G>A (p.Gly191Asp) rs2534611135
NM_006774.5(INMT):c.593C>T (p.Thr198Met)
NM_006774.5(INMT):c.657G>T (p.Glu219Asp) rs2534611571
NM_006774.5(INMT):c.703C>T (p.Leu235Phe)
NM_006774.5(INMT):c.720G>C (p.Gln240His) rs1355183880
NM_006774.5(INMT):c.746A>G (p.Asn249Ser)
NM_006774.5(INMT):c.772C>G (p.Arg258Gly) rs150713465
NM_006774.5(INMT):c.773G>T (p.Arg258Leu) rs6970605
NM_006774.5(INMT):c.98C>A (p.Pro33His) rs754241642

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.