ClinVar Miner

List of variants in gene RET reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 100
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe) rs77724903 0.00178
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.1124T>A (p.Leu375Gln) rs142338976 0.00073
NM_020975.6(RET):c.262A>G (p.Ile88Val) rs141679950 0.00056
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala) rs201740483 0.00047
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214 0.00039
NM_020975.6(RET):c.2037C>T (p.Pro679=) rs55862116 0.00039
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.785T>C (p.Val262Ala) rs139790943 0.00024
NM_020975.6(RET):c.874G>A (p.Val292Met) rs34682185 0.00023
NM_020975.6(RET):c.3040-20C>T rs372172456 0.00020
NM_020975.6(RET):c.1529C>T (p.Ala510Val) rs201745826 0.00019
NM_020975.6(RET):c.2052G>A (p.Pro684=) rs145122337 0.00019
NM_020975.6(RET):c.2607+4C>T rs200634990 0.00015
NM_020975.6(RET):c.1063+9G>A rs765463636 0.00014
NM_020975.6(RET):c.1668C>G (p.Ser556=) rs141771814 0.00014
NM_020975.6(RET):c.1699G>A (p.Asp567Asn) rs147219360 0.00014
NM_020975.6(RET):c.1701C>T (p.Asp567=) rs201209972 0.00014
NM_020975.6(RET):c.2988G>A (p.Pro996=) rs145798106 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.337+11C>T rs754967305 0.00011
NM_020975.6(RET):c.957C>A (p.Leu319=) rs149926238 0.00011
NM_020975.6(RET):c.2136+15G>A rs751183869 0.00009
NM_020975.6(RET):c.1879+13C>T rs375573788 0.00008
NM_020975.6(RET):c.2081G>A (p.Arg694Gln) rs141185224 0.00008
NM_020975.6(RET):c.1942G>A (p.Val648Ile) rs77711105 0.00007
NM_020975.6(RET):c.2409C>T (p.Ile803=) rs535051804 0.00006
NM_020975.6(RET):c.2607+3G>A rs752538741 0.00006
NM_020975.6(RET):c.2742A>G (p.Pro914=) rs375963128 0.00006
NM_020975.6(RET):c.1476C>G (p.Thr492=) rs758249079 0.00005
NM_020975.6(RET):c.1064-6C>T rs768878280 0.00004
NM_020975.6(RET):c.1118C>T (p.Ala373Val) rs546866208 0.00004
NM_020975.6(RET):c.2139G>A (p.Glu713=) rs149460492 0.00004
NM_020975.6(RET):c.1760-12G>A rs377767392 0.00003
NM_020975.6(RET):c.3060G>A (p.Ala1020=) rs767152839 0.00003
NM_020975.6(RET):c.3138C>A (p.Ala1046=) rs201576838 0.00003
NM_020975.6(RET):c.582G>A (p.Gln194=) rs368116579 0.00003
NM_020975.6(RET):c.626-4G>A rs775956924 0.00003
NM_020975.6(RET):c.897C>T (p.Phe299=) rs529153319 0.00003
NM_020975.6(RET):c.1264-4C>T rs587780806 0.00002
NM_020975.6(RET):c.144G>A (p.Thr48=) rs759872307 0.00002
NM_020975.6(RET):c.1522+17G>A rs760269666 0.00002
NM_020975.6(RET):c.1695C>T (p.Cys565=) rs775079681 0.00002
NM_020975.6(RET):c.1914C>T (p.Ile638=) rs375041479 0.00002
NM_020975.6(RET):c.1920C>T (p.Ala640=) rs149768519 0.00002
NM_020975.6(RET):c.2939+6C>T rs181245759 0.00002
NM_020975.6(RET):c.868-9A>G rs201766252 0.00002
NM_020975.6(RET):c.1029C>T (p.Asn343=) rs764668178 0.00001
NM_020975.6(RET):c.1063+20C>T rs769558279 0.00001
NM_020975.6(RET):c.1264-8C>T rs769595884 0.00001
NM_020975.6(RET):c.1266C>T (p.Ile422=) rs759582152 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.1539G>A (p.Ala513=) rs761430718 0.00001
NM_020975.6(RET):c.1908G>A (p.Thr636=) rs886038663 0.00001
NM_020975.6(RET):c.1926C>G (p.Val642=) rs766962871 0.00001
NM_020975.6(RET):c.1956G>A (p.Leu652=) rs954292063 0.00001
NM_020975.6(RET):c.2079C>G (p.Arg693=) rs747166722 0.00001
NM_020975.6(RET):c.2289C>T (p.Asn763=) rs777349208 0.00001
NM_020975.6(RET):c.2607+24C>T rs779255047 0.00001
NM_020975.6(RET):c.2802-4G>T rs878855061 0.00001
NM_020975.6(RET):c.3057G>A (p.Ala1019=) rs369579749 0.00001
NM_020975.6(RET):c.322A>C (p.Lys108Gln) rs567877611 0.00001
NM_020975.6(RET):c.45G>A (p.Leu15=) rs876660157 0.00001
NM_020975.6(RET):c.625+9C>T rs201453349 0.00001
NM_020975.6(RET):c.750C>T (p.Arg250=) rs1013952995 0.00001
NM_020975.6(RET):c.*6C>G
NM_020975.6(RET):c.1416C>G (p.Ala472=) rs1564494451
NM_020975.6(RET):c.1470G>A (p.Gln490=) rs1564494516
NM_020975.6(RET):c.1522+30G>A
NM_020975.6(RET):c.1522+41G>T
NM_020975.6(RET):c.1522+42dup
NM_020975.6(RET):c.1523-7C>T rs567967877
NM_020975.6(RET):c.153G>A (p.Leu51=) rs1837615966
NM_020975.6(RET):c.1821C>T (p.Gly607=) rs1837993502
NM_020975.6(RET):c.2049C>T (p.Phe683=) rs2132851661
NM_020975.6(RET):c.2136+9C>T rs1331402266
NM_020975.6(RET):c.2284+26C>T
NM_020975.6(RET):c.2284+54C>T
NM_020975.6(RET):c.231C>T (p.Arg77=) rs3123654
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.2731-8C>G rs1564499958
NM_020975.6(RET):c.3123G>A (p.Val1041=) rs147437610
NM_020975.6(RET):c.3135T>C (p.Asn1045=) rs1217348681
NM_020975.6(RET):c.3141C>G (p.Pro1047=) rs372673589
NM_020975.6(RET):c.3187+37G>C
NM_020975.6(RET):c.351C>T (p.Pro117=) rs267602487
NM_020975.6(RET):c.487C>A (p.Arg163=) rs371153966
NM_020975.6(RET):c.624G>T (p.Glu208Asp) rs781750106
NM_020975.6(RET):c.633T>C (p.Gly211=) rs1371983599
NM_020975.6(RET):c.951G>A (p.Thr317=) rs375812189

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.