ClinVar Miner

List of variants in gene RET reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.405C>T (p.Gly135=) rs142345108 0.00051
NM_020975.6(RET):c.341G>A (p.Arg114His) rs76397662 0.00039
NM_020975.6(RET):c.1531G>A (p.Glu511Lys) rs201553718 0.00018
NM_020975.6(RET):c.1344C>G (p.Asn448Lys) rs549907428 0.00011
NM_020975.6(RET):c.1642G>A (p.Gly548Ser) rs374461212 0.00011
NM_020975.6(RET):c.2556C>G (p.Ile852Met) rs377767426 0.00011
NM_020975.6(RET):c.961G>A (p.Gly321Arg) rs377767388 0.00009
NM_020975.6(RET):c.2527G>A (p.Glu843Lys) rs755837568 0.00006
NM_020975.6(RET):c.604G>A (p.Val202Met) rs751572082 0.00006
NM_020975.6(RET):c.1103G>A (p.Arg368His) rs199529397 0.00005
NM_020975.6(RET):c.3059C>T (p.Ala1020Val) rs372191563 0.00005
NM_020975.6(RET):c.1420C>T (p.Arg474Trp) rs775842917 0.00004
NM_020975.6(RET):c.2477A>C (p.Tyr826Ser) rs34617196 0.00004
NM_020975.6(RET):c.406G>A (p.Glu136Lys) rs79014735 0.00004
NM_020975.6(RET):c.1083C>A (p.Asn361Lys) rs770587835 0.00003
NM_020975.6(RET):c.1312G>A (p.Val438Ile) rs774474422 0.00003
NM_020975.6(RET):c.1573C>T (p.Arg525Trp) rs545625150 0.00003
NM_020975.6(RET):c.1724C>T (p.Thr575Ile) rs587780808 0.00003
NM_020975.6(RET):c.1737C>G (p.Asn579Lys) rs144455821 0.00003
NM_020975.6(RET):c.2656C>T (p.Arg886Trp) rs146838520 0.00003
NM_020975.6(RET):c.2931C>G (p.Ser977Arg) rs375414982 0.00003
NM_020975.6(RET):c.3149G>A (p.Arg1050Gln) rs200956659 0.00003
NM_020975.6(RET):c.170G>A (p.Arg57Gln) rs779915615 0.00002
NM_020975.6(RET):c.2488G>A (p.Gly830Arg) rs200127630 0.00002
NM_020975.6(RET):c.2755G>C (p.Ala919Pro) rs1361265737 0.00002
NM_020975.6(RET):c.304G>A (p.Asp102Asn) rs201244749 0.00002
NM_020975.6(RET):c.3233C>T (p.Thr1078Met) rs762952212 0.00002
NM_020975.6(RET):c.682G>C (p.Ala228Pro) rs760813493 0.00002
NM_020975.6(RET):c.1008C>G (p.Asn336Lys) rs144981275 0.00001
NM_020975.6(RET):c.1076A>G (p.Asn359Ser) rs1204350955 0.00001
NM_020975.6(RET):c.1151C>G (p.Pro384Arg) rs771679592 0.00001
NM_020975.6(RET):c.1367C>T (p.Thr456Ile) rs1286634866 0.00001
NM_020975.6(RET):c.1811C>T (p.Ala604Val) rs1286776938 0.00001
NM_020975.6(RET):c.1907C>T (p.Thr636Met) rs1035958105 0.00001
NM_020975.6(RET):c.1915G>A (p.Ala639Thr) rs777122776 0.00001
NM_020975.6(RET):c.2080C>T (p.Arg694Trp) rs193922700 0.00001
NM_020975.6(RET):c.2249C>G (p.Ala750Gly) rs752830000 0.00001
NM_020975.6(RET):c.2437C>T (p.Arg813Trp) rs779996040 0.00001
NM_020975.6(RET):c.2438G>A (p.Arg813Gln) rs1318733775 0.00001
NM_020975.6(RET):c.2662A>G (p.Met888Val) rs774930499 0.00001
NM_020975.6(RET):c.2716G>A (p.Val906Met) rs200627072 0.00001
NM_020975.6(RET):c.2815G>A (p.Val939Ile) rs1554819950 0.00001
NM_020975.6(RET):c.3044A>G (p.Tyr1015Cys) rs1438192223 0.00001
NM_020975.6(RET):c.3093C>T (p.Asp1031=) rs369116900 0.00001
NM_020975.6(RET):c.3148C>G (p.Arg1050Gly) rs767479170 0.00001
NM_020975.6(RET):c.3184T>C (p.Tyr1062His) rs138010639 0.00001
NM_020975.6(RET):c.3326T>C (p.Met1109Thr) rs587780813 0.00001
NM_020975.6(RET):c.340C>T (p.Arg114Cys) rs747483905 0.00001
NM_020975.6(RET):c.463C>T (p.Pro155Ser) rs1356388972 0.00001
NM_020975.6(RET):c.602G>C (p.Ser201Thr) rs898525501 0.00001
NM_020975.6(RET):c.628G>A (p.Glu210Lys) rs1060500762 0.00001
NM_020975.6(RET):c.884C>T (p.Thr295Met) rs758159521 0.00001
NM_020975.6(RET):c.943A>C (p.Thr315Pro) rs774637214 0.00001
NM_020975.6(RET):c.1078C>A (p.Arg360=) rs1424549058
NM_020975.6(RET):c.1198G>A (p.Val400Ile)
NM_020975.6(RET):c.1207C>T (p.His403Tyr) rs1449633271
NM_020975.6(RET):c.1295_1296inv (p.Ala432Val)
NM_020975.6(RET):c.1299C>G (p.Phe433Leu) rs1554818526
NM_020975.6(RET):c.1569G>T (p.Lys523Asn) rs751464792
NM_020975.6(RET):c.1609C>T (p.Pro537Ser) rs1438717389
NM_020975.6(RET):c.1657_1671del (p.Arg553_Thr557del)
NM_020975.6(RET):c.1867G>C (p.Glu623Gln)
NM_020975.6(RET):c.1921G>T (p.Ala641Ser) rs377767411
NM_020975.6(RET):c.2100G>A (p.Met700Ile) rs1564496551
NM_020975.6(RET):c.2140G>A (p.Asp714Asn) rs2132902537
NM_020975.6(RET):c.2209A>C (p.Lys737Gln) rs768217520
NM_020975.6(RET):c.2348A>C (p.Asn783Thr) rs587778656
NM_020975.6(RET):c.2571G>T (p.Gln857His) rs1588877374
NM_020975.6(RET):c.2870C>G (p.Pro957Arg) rs1259087541
NM_020975.6(RET):c.2909T>C (p.Met970Thr)
NM_020975.6(RET):c.2939+5G>A rs2538617530
NM_020975.6(RET):c.2994T>G (p.Phe998Leu) rs2538626999
NM_020975.6(RET):c.2996C>G (p.Ala999Gly) rs748288493
NM_020975.6(RET):c.3039A>T (p.Arg1013Ser)
NM_020975.6(RET):c.3187+1G>C rs1233945445
NM_020975.6(RET):c.3335T>C (p.Phe1112Ser) rs756449491
NM_020975.6(RET):c.443_445del (p.Ser148del) rs2492157382
NM_020975.6(RET):c.613A>G (p.Arg205Gly) rs1564490234
NM_020975.6(RET):c.650C>A (p.Ala217Asp) rs1060500754
NM_020975.6(RET):c.931G>T (p.Val311Leu) rs1311500725
NM_020975.6(RET):c.950C>T (p.Thr317Met) rs760322514
NM_020975.6(RET):c.95C>G (p.Ser32Trp)
NM_020975.6(RET):c.983C>A (p.Thr328Asn)

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