ClinVar Miner

List of variants in gene RET reported as likely benign by Sema4, Sema4

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958 0.00310
NM_020975.6(RET):c.468C>T (p.Ala156=) rs141290380 0.00173
NM_020975.6(RET):c.654G>A (p.Pro218=) rs137928436 0.00138
NM_020975.6(RET):c.1197G>A (p.Pro399=) rs148371113 0.00108
NM_020975.6(RET):c.1157C>T (p.Ala386Val) rs115272158 0.00101
NM_020975.6(RET):c.1119G>A (p.Ala373=) rs113931414 0.00079
NM_020975.6(RET):c.262A>G (p.Ile88Val) rs141679950 0.00056
NM_020975.6(RET):c.225G>A (p.Thr75=) rs151267865 0.00052
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala) rs201740483 0.00047
NM_020975.6(RET):c.1354C>A (p.Leu452Ile) rs151148041 0.00043
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214 0.00039
NM_020975.6(RET):c.200G>A (p.Arg67His) rs192489011 0.00036
NM_020975.6(RET):c.1050C>T (p.Thr350=) rs142188675 0.00031
NM_020975.6(RET):c.2673G>A (p.Ser891=) rs201620214 0.00027
NM_020975.6(RET):c.2943C>T (p.Tyr981=) rs147318495 0.00024
NM_020975.6(RET):c.2052G>A (p.Pro684=) rs145122337 0.00019
NM_020975.6(RET):c.1017G>A (p.Ser339=) rs369810881 0.00014
NM_020975.6(RET):c.1699G>A (p.Asp567Asn) rs147219360 0.00014
NM_020975.6(RET):c.868-6C>T rs367688294 0.00013
NM_020975.6(RET):c.1437C>T (p.Ala479=) rs576806356 0.00011
NM_020975.6(RET):c.1522+35C>T rs377130948 0.00011
NM_020975.6(RET):c.2601G>T (p.Glu867Asp) rs141459368 0.00011
NM_020975.6(RET):c.957C>A (p.Leu319=) rs149926238 0.00011
NM_020975.6(RET):c.1866C>G (p.Pro622=) rs201979255 0.00010
NM_020975.6(RET):c.3156C>T (p.Leu1052=) rs191769748 0.00008
NM_020975.6(RET):c.1942G>A (p.Val648Ile) rs77711105 0.00007
NM_020975.6(RET):c.81G>A (p.Leu27=) rs369519655 0.00007
NM_020975.6(RET):c.3142C>T (p.Leu1048Phe) rs774347808 0.00006
NM_020975.6(RET):c.816C>T (p.Phe272=) rs754428451 0.00006
NM_020975.6(RET):c.3188-9C>T rs551159582 0.00005
NM_020975.6(RET):c.1438G>A (p.Glu480Lys) rs537874538 0.00004
NM_020975.6(RET):c.2139G>A (p.Glu713=) rs149460492 0.00004
NM_020975.6(RET):c.693C>T (p.Arg231=) rs576806329 0.00004
NM_020975.6(RET):c.1878G>A (p.Gln626=) rs147692872 0.00003
NM_020975.6(RET):c.2298G>A (p.Pro766=) rs140658743 0.00003
NM_020975.6(RET):c.3138C>A (p.Ala1046=) rs201576838 0.00003
NM_020975.6(RET):c.46C>T (p.Leu16=) rs1309896929 0.00003
NM_020975.6(RET):c.1941C>T (p.Ile647=) rs75225191 0.00002
NM_020975.6(RET):c.2226G>A (p.Thr742=) rs762876946 0.00002
NM_020975.6(RET):c.2393-9C>T rs567543719 0.00002
NM_020975.6(RET):c.2505C>T (p.Ser835=) rs1060504033 0.00002
NM_020975.6(RET):c.1047G>A (p.Ala349=) rs373208682 0.00001
NM_020975.6(RET):c.1374C>T (p.Ala458=) rs190750926 0.00001
NM_020975.6(RET):c.1386G>A (p.Ser462=) rs587780807 0.00001
NM_020975.6(RET):c.1464C>T (p.Thr488=) rs921948385 0.00001
NM_020975.6(RET):c.1710C>T (p.Cys570=) rs144015580 0.00001
NM_020975.6(RET):c.2715C>T (p.Tyr905=) rs755023496 0.00001
NM_020975.6(RET):c.322A>C (p.Lys108Gln) rs567877611 0.00001
NM_020975.6(RET):c.1161C>T (p.Gly387=) rs763967472
NM_020975.6(RET):c.2029C>A (p.Arg677=) rs1432069386
NM_020975.6(RET):c.2199C>T (p.Gly733=) rs587780809
NM_020975.6(RET):c.2284+54C>A rs566375223
NM_020975.6(RET):c.2448C>T (p.Leu816=) rs368500000
NM_020975.6(RET):c.2454G>A (p.Glu818=) rs794727131
NM_020975.6(RET):c.2523G>A (p.Pro841=) rs56195026
NM_020975.6(RET):c.2523G>T (p.Pro841=) rs56195026
NM_020975.6(RET):c.3036G>A (p.Arg1012=) rs1196348217
NM_020975.6(RET):c.487C>A (p.Arg163=) rs371153966
NM_020975.6(RET):c.786G>A (p.Val262=) rs1060504035

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.