ClinVar Miner

List of variants in gene MYBPC3 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 131
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HGVS dbSNP
NM_000256.3(MYBPC3):c.-5T>C rs886048383
NM_000256.3(MYBPC3):c.1008C>T (p.Ile336=) rs397515880
NM_000256.3(MYBPC3):c.1062C>A (p.Gly354=) rs1555122748
NM_000256.3(MYBPC3):c.1091-197G>T
NM_000256.3(MYBPC3):c.1091-39C>T
NM_000256.3(MYBPC3):c.1149G>T (p.Leu383=) rs1407534196
NM_000256.3(MYBPC3):c.1224-3C>T rs1555122359
NM_000256.3(MYBPC3):c.1227-18C>A
NM_000256.3(MYBPC3):c.1227-4C>G rs113628269
NM_000256.3(MYBPC3):c.1302C>T (p.Tyr434=)
NM_000256.3(MYBPC3):c.1352-10G>T rs745645848
NM_000256.3(MYBPC3):c.1374C>T (p.Arg458=) rs1057521555
NM_000256.3(MYBPC3):c.1422G>A (p.Glu474=) rs397515901
NM_000256.3(MYBPC3):c.1434G>A (p.Ser478=) rs770568659
NM_000256.3(MYBPC3):c.1458-5G>A rs746542705
NM_000256.3(MYBPC3):c.1467C>T (p.Asp489=) rs35690719
NM_000256.3(MYBPC3):c.147C>T (p.Ile49=) rs774273586
NM_000256.3(MYBPC3):c.148A>G (p.Ser50Gly) rs373164247
NM_000256.3(MYBPC3):c.1519G>A (p.Gly507Arg) rs35736435
NM_000256.3(MYBPC3):c.1563C>T (p.Asp521=) rs367915627
NM_000256.3(MYBPC3):c.1564G>A (p.Ala522Thr) rs11570082
NM_000256.3(MYBPC3):c.1593G>A (p.Gly531=) rs727503199
NM_000256.3(MYBPC3):c.1624+13G>A rs397515913
NM_000256.3(MYBPC3):c.1624+13G>C rs397515913
NM_000256.3(MYBPC3):c.1624+14_1624+15insA rs369096037
NM_000256.3(MYBPC3):c.1624+18G>C rs767468093
NM_000256.3(MYBPC3):c.1759G>A (p.Asp587Asn) rs730880526
NM_000256.3(MYBPC3):c.1791-8C>T rs1346693579
NM_000256.3(MYBPC3):c.1830C>T (p.Asp610=)
NM_000256.3(MYBPC3):c.1855G>A (p.Glu619Lys) rs200352299
NM_000256.3(MYBPC3):c.1857G>A (p.Glu619=)
NM_000256.3(MYBPC3):c.1860C>G (p.Gly620=)
NM_000256.3(MYBPC3):c.1881C>A (p.Ala627=) rs1555121890
NM_000256.3(MYBPC3):c.1897+47G>A
NM_000256.3(MYBPC3):c.1927+16C>G rs1057521019
NM_000256.3(MYBPC3):c.1928-19T>A rs1057521020
NM_000256.3(MYBPC3):c.1935C>T (p.Pro645=) rs727503193
NM_000256.3(MYBPC3):c.1944C>T (p.His648=) rs750861887
NM_000256.3(MYBPC3):c.1968A>G (p.Pro656=) rs397515940
NM_000256.3(MYBPC3):c.2010C>T (p.Asp670=) rs558051480
NM_000256.3(MYBPC3):c.2068-12C>G
NM_000256.3(MYBPC3):c.207G>C (p.Arg69=) rs397515946
NM_000256.3(MYBPC3):c.2149-3C>T rs113182334
NM_000256.3(MYBPC3):c.216C>A (p.Gly72=) rs760007714
NM_000256.3(MYBPC3):c.2250G>A (p.Thr750=) rs373338699
NM_000256.3(MYBPC3):c.2271G>A (p.Val757=) rs766029254
NM_000256.3(MYBPC3):c.2308+13G>A rs780086088
NM_000256.3(MYBPC3):c.2309-96C>G
NM_000256.3(MYBPC3):c.2309-9C>A rs730880528
NM_000256.3(MYBPC3):c.2310C>T (p.Asp770=) rs397515959
NM_000256.3(MYBPC3):c.2346C>T (p.Asn782=) rs768638405
NM_000256.3(MYBPC3):c.2397C>T (p.Gly799=) rs756512665
NM_000256.3(MYBPC3):c.2409C>A (p.Ile803=) rs202088839
NM_000256.3(MYBPC3):c.240A>G (p.Ala80=) rs770089112
NM_000256.3(MYBPC3):c.2413+14C>T
NM_000256.3(MYBPC3):c.2413+18G>C rs768281173
NM_000256.3(MYBPC3):c.2497G>A (p.Ala833Thr) rs199865688
NM_000256.3(MYBPC3):c.2517C>T (p.Gly839=) rs370561202
NM_000256.3(MYBPC3):c.2544G>A (p.Ala848=) rs369904619
NM_000256.3(MYBPC3):c.2556C>T (p.Ile852=) rs754062873
NM_000256.3(MYBPC3):c.2568G>A (p.Arg856=) rs773032022
NM_000256.3(MYBPC3):c.26+13C>T rs756818187
NM_000256.3(MYBPC3):c.2602+9G>A rs960769310
NM_000256.3(MYBPC3):c.2603-11C>T rs11570105
NM_000256.3(MYBPC3):c.2613C>T (p.Ser871=) rs531228202
NM_000256.3(MYBPC3):c.2614G>A (p.Glu872Lys) rs190765116
NM_000256.3(MYBPC3):c.2622C>T (p.Thr874=) rs886048375
NM_000256.3(MYBPC3):c.2733G>A (p.Glu911=) rs1385242275
NM_000256.3(MYBPC3):c.2761C>G (p.Gln921Glu) rs367729718
NM_000256.3(MYBPC3):c.2808G>A (p.Thr936=) rs370530334
NM_000256.3(MYBPC3):c.2838A>G (p.Ala946=) rs376858768
NM_000256.3(MYBPC3):c.2870C>G (p.Thr957Ser) rs193922380
NM_000256.3(MYBPC3):c.2873C>T (p.Thr958Ile) rs376504548
NM_000256.3(MYBPC3):c.2895G>A (p.Gln965=) rs1057524069
NM_000256.3(MYBPC3):c.2905+9C>T rs1057520951
NM_000256.3(MYBPC3):c.2906-9T>C
NM_000256.3(MYBPC3):c.2914C>T (p.Arg972Trp) rs193922382
NM_000256.3(MYBPC3):c.2995-5C>G rs376083315
NM_000256.3(MYBPC3):c.3057G>A (p.Val1019=) rs750618688
NM_000256.3(MYBPC3):c.3097C>A (p.Arg1033=) rs748909815
NM_000256.3(MYBPC3):c.3106C>T (p.Arg1036Cys) rs61729664
NM_000256.3(MYBPC3):c.3108C>A (p.Arg1036=) rs747059136
NM_000256.3(MYBPC3):c.3168C>T (p.Ala1056=) rs373208282
NM_000256.3(MYBPC3):c.3191-9C>T rs1316069252
NM_000256.3(MYBPC3):c.3229G>A (p.Ala1077Thr) rs397516009
NM_000256.3(MYBPC3):c.3264A>G (p.Pro1088=) rs758229677
NM_000256.3(MYBPC3):c.3279C>T (p.Gly1093=) rs36212064
NM_000256.3(MYBPC3):c.332C>T (p.Ala111Val) rs730880530
NM_000256.3(MYBPC3):c.3362G>A (p.Arg1121His) rs397516018
NM_000256.3(MYBPC3):c.3392T>C (p.Ile1131Thr) rs370890951
NM_000256.3(MYBPC3):c.3431T>C (p.Met1144Thr) rs730880529
NM_000256.3(MYBPC3):c.3472G>A (p.Val1158Ile) rs542350927
NM_000256.3(MYBPC3):c.3579C>T (p.Ile1193=)
NM_000256.3(MYBPC3):c.3627+14G>A rs1057521242
NM_000256.3(MYBPC3):c.3628-6T>C rs1057520329
NM_000256.3(MYBPC3):c.363G>A (p.Pro121=) rs780768974
NM_000256.3(MYBPC3):c.3708G>A (p.Leu1236=) rs767400149
NM_000256.3(MYBPC3):c.372C>T (p.Ala124=) rs11570046
NM_000256.3(MYBPC3):c.3777G>A (p.Gln1259=) rs746042492
NM_000256.3(MYBPC3):c.3801C>T (p.Arg1267=) rs541377415
NM_000256.3(MYBPC3):c.3814+13C>A rs764528392
NM_000256.3(MYBPC3):c.3816G>A (p.Val1272=) rs776112819
NM_000256.3(MYBPC3):c.408G>C (p.Gly136=) rs1057520977
NM_000256.3(MYBPC3):c.418G>C (p.Ala140Pro) rs730880614
NM_000256.3(MYBPC3):c.440C>T (p.Pro147Leu) rs730880615
NM_000256.3(MYBPC3):c.505+9G>A
NM_000256.3(MYBPC3):c.540C>T (p.Gly180=) rs371842442
NM_000256.3(MYBPC3):c.567C>G (p.Val189=) rs1290069260
NM_000256.3(MYBPC3):c.639C>T (p.Tyr213=) rs727504858
NM_000256.3(MYBPC3):c.646G>A (p.Ala216Thr) rs201098973
NM_000256.3(MYBPC3):c.648C>T (p.Ala216=) rs777418402
NM_000256.3(MYBPC3):c.654+17C>T rs369864892
NM_000256.3(MYBPC3):c.655-15C>T rs188327777
NM_000256.3(MYBPC3):c.771C>T (p.His257=)
NM_000256.3(MYBPC3):c.772+215G>C
NM_000256.3(MYBPC3):c.772+9G>T rs566339669
NM_000256.3(MYBPC3):c.799C>G (p.Leu267Val) rs370941975
NM_000256.3(MYBPC3):c.81C>T (p.Ala27=) rs761547225
NM_000256.3(MYBPC3):c.821+13C>G rs1057521528
NM_000256.3(MYBPC3):c.851+17C>A
NM_000256.3(MYBPC3):c.851+18C>T rs377287239
NM_000256.3(MYBPC3):c.852-10C>G rs750425291
NM_000256.3(MYBPC3):c.882C>T (p.Asp294=) rs1459586065
NM_000256.3(MYBPC3):c.905+11G>T rs1025510303
NM_000256.3(MYBPC3):c.908+13G>A rs1321998052
NM_000256.3(MYBPC3):c.921C>A (p.Thr307=) rs370632180
NM_000256.3(MYBPC3):c.926+25C>A
NM_000256.3(MYBPC3):c.927-10C>G rs201078659
NM_000256.3(MYBPC3):c.927-10C>T rs201078659
NM_000256.3(MYBPC3):c.927-20G>A
NM_000256.3(MYBPC3):c.960C>T (p.Asp320=) rs369900803

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