ClinVar Miner

List of variants in gene RET reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.1063+47G>A rs372177579 0.00315
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958 0.00310
NM_020975.6(RET):c.1336G>C (p.Gly446Arg) rs115423919 0.00238
NM_020975.6(RET):c.337+12G>A rs200468424 0.00198
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe) rs77724903 0.00178
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.626-41G>A rs572623103 0.00098
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.833C>A (p.Thr278Asn) rs35118262 0.00056
NM_020975.6(RET):c.225G>A (p.Thr75=) rs151267865 0.00052
NM_020975.6(RET):c.*29C>A rs199639914 0.00050
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.200G>A (p.Arg67His) rs192489011 0.00036
NM_020975.6(RET):c.1158G>A (p.Ala386=) rs373540097 0.00034
NM_020975.6(RET):c.2673G>A (p.Ser891=) rs201620214 0.00027
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.2052G>A (p.Pro684=) rs145122337 0.00019
NM_020975.6(RET):c.1531G>A (p.Glu511Lys) rs201553718 0.00018
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.1701C>T (p.Asp567=) rs201209972 0.00014
NM_020975.6(RET):c.2988G>A (p.Pro996=) rs145798106 0.00014
NM_020975.6(RET):c.1893C>T (p.Asp631=) rs55846256 0.00013
NM_020975.6(RET):c.868-6C>T rs367688294 0.00013
NM_020975.6(RET):c.398G>A (p.Arg133His) rs138265837 0.00012
NM_020975.6(RET):c.597C>T (p.Asn199=) rs55810667 0.00012
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.2940-45C>T rs370072408 0.00009
NM_020975.6(RET):c.2611G>A (p.Val871Ile) rs145170911 0.00008
NM_020975.6(RET):c.1942G>A (p.Val648Ile) rs77711105 0.00007
NM_020975.6(RET):c.2418C>T (p.Tyr806=) rs553418132 0.00005
NM_020975.6(RET):c.3188-9C>T rs551159582 0.00005
NM_020975.6(RET):c.1118C>T (p.Ala373Val) rs546866208 0.00004
NM_020975.6(RET):c.2976G>A (p.Pro992=) rs528823385 0.00004
NM_020975.6(RET):c.3090C>T (p.Asp1030=) rs142859395 0.00003
NM_020975.6(RET):c.582G>A (p.Gln194=) rs368116579 0.00003
NM_020975.6(RET):c.2358T>C (p.His786=) rs758715544 0.00002
NM_020975.6(RET):c.2802-11A>T rs1220802134 0.00002
NM_020975.6(RET):c.342C>T (p.Arg114=) rs143083395 0.00002
NM_020975.6(RET):c.777G>A (p.Pro259=) rs1279646689 0.00002
NM_020975.6(RET):c.1029C>T (p.Asn343=) rs764668178 0.00001
NM_020975.6(RET):c.1221C>T (p.Thr407=) rs1222385123 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.1522+20A>G rs1053383471 0.00001
NM_020975.6(RET):c.1890C>T (p.Cys630=) rs781145070 0.00001
NM_020975.6(RET):c.1908G>A (p.Thr636=) rs886038663 0.00001
NM_020975.6(RET):c.2538C>T (p.Leu846=) rs201816539 0.00001
NM_020975.6(RET):c.2547C>T (p.Gly849=) rs770674650 0.00001
NM_020975.6(RET):c.2607+24C>T rs779255047 0.00001
NM_020975.6(RET):c.2730+12C>T rs372080924 0.00001
NM_020975.6(RET):c.2939+20G>A rs201756161 0.00001
NM_020975.6(RET):c.3057G>A (p.Ala1019=) rs369579749 0.00001
NM_020975.6(RET):c.626-49C>T rs1381620754 0.00001
NM_020975.6(RET):c.1064-22A>G
NM_020975.6(RET):c.1146G>A (p.Gln382=) rs770637118
NM_020975.6(RET):c.1264-43C>T
NM_020975.6(RET):c.1353G>A (p.Thr451=) rs201568301
NM_020975.6(RET):c.1522+20A>T
NM_020975.6(RET):c.1523-12T>G rs1429462039
NM_020975.6(RET):c.2262G>A (p.Thr754=) rs779080598
NM_020975.6(RET):c.2284+54C>A rs566375223
NM_020975.6(RET):c.2393-14C>T rs144269978
NM_020975.6(RET):c.2393-29C>T
NM_020975.6(RET):c.2393-5C>T rs1554819512
NM_020975.6(RET):c.2523G>T (p.Pro841=) rs56195026
NM_020975.6(RET):c.337+20A>C
NM_020975.6(RET):c.337+24A>C rs1364998745
NM_020975.6(RET):c.44TGC[8] (p.Leu19_Pro20insLeuLeuLeu) rs768132465
NM_020975.6(RET):c.626-21C>T
NM_020975.6(RET):c.951G>A (p.Thr317=) rs375812189

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