ClinVar Miner

List of variants in gene MEN1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP
NM_000244.3(MEN1):c.*16G>A rs140924477
NM_000244.3(MEN1):c.1064+9C>T rs200517349
NM_000244.3(MEN1):c.1089G>A (p.Glu363=) rs776834299
NM_000244.3(MEN1):c.1206C>T (p.Thr402=) rs1166154585
NM_000244.3(MEN1):c.1221C>A (p.Ser407=) rs770037856
NM_000244.3(MEN1):c.1311G>A (p.Leu437=) rs138770431
NM_000244.3(MEN1):c.1366-4C>T rs764408631
NM_000244.3(MEN1):c.1401C>G (p.Ala467=) rs771827808
NM_000244.3(MEN1):c.1419G>A (p.Glu473=) rs755734265
NM_000244.3(MEN1):c.1425G>A (p.Pro475=) rs1060503795
NM_000244.3(MEN1):c.1458G>A (p.Arg486=) rs864622641
NM_000244.3(MEN1):c.162C>T (p.Ile54=) rs1555166662
NM_000244.3(MEN1):c.1653G>A (p.Pro551=) rs368783097
NM_000244.3(MEN1):c.165T>A (p.Pro55=) rs1060503790
NM_000244.3(MEN1):c.1671T>C (p.Thr557=) rs143423552
NM_000244.3(MEN1):c.1710G>T (p.Leu570=) rs767677287
NM_000244.3(MEN1):c.1716C>T (p.Ala572=) rs757417271
NM_000244.3(MEN1):c.1755G>C (p.Thr585=) rs1114167530
NM_000244.3(MEN1):c.1764G>C (p.Ser588=) rs765105348
NM_000244.3(MEN1):c.1773G>A (p.Gln591=) rs759563305
NM_000244.3(MEN1):c.177C>G (p.Pro59=) rs749001511
NM_000244.3(MEN1):c.1821C>T (p.Phe607=) rs1060503794
NM_000244.3(MEN1):c.300C>G (p.Ala100=) rs773136972
NM_000244.3(MEN1):c.330G>C (p.Gly110=) rs1060503792
NM_000244.3(MEN1):c.48C>T (p.Ile16=) rs1060503797
NM_000244.3(MEN1):c.636G>A (p.Arg212=) rs779966911
NM_000244.3(MEN1):c.768C>T (p.Thr256=) rs763326062
NM_000244.3(MEN1):c.774G>T (p.Ser258=) rs201829546
NM_000244.3(MEN1):c.777G>A (p.Leu259=) rs199909967
NM_000244.3(MEN1):c.798+7G>A rs1060503793
NM_001370259.2(MEN1):c.102G>A (p.Leu34=) rs1255708093
NM_001370259.2(MEN1):c.1059C>T (p.Tyr353=) rs1592640846
NM_001370259.2(MEN1):c.1062C>T (p.Cys354=) rs104894265
NM_001370259.2(MEN1):c.1065G>C (p.Arg355=) rs1592640719
NM_001370259.2(MEN1):c.108C>G (p.Leu36=) rs1592660352
NM_001370259.2(MEN1):c.1095T>C (p.Phe365=) rs1592640464
NM_001370259.2(MEN1):c.1119C>T (p.Pro373=) rs535417698
NM_001370259.2(MEN1):c.1158C>G (p.Gly386=) rs794728653
NM_001370259.2(MEN1):c.1173G>A (p.Gly391=) rs1592639850
NM_001370259.2(MEN1):c.120G>T (p.Val40=) rs1306316325
NM_001370259.2(MEN1):c.1356G>A (p.Arg452=) rs1180957953
NM_001370259.2(MEN1):c.1467A>G (p.Pro489=) rs1592632826
NM_001370259.2(MEN1):c.1479G>T (p.Pro493=) rs546721780
NM_001370259.2(MEN1):c.156C>A (p.Arg52=) rs1592659960
NM_001370259.2(MEN1):c.1584C>G (p.Gly528=) rs1592631208
NM_001370259.2(MEN1):c.159C>T (p.Val53=) rs1411927545
NM_001370259.2(MEN1):c.1602G>A (p.Thr534=) rs1592631034
NM_001370259.2(MEN1):c.1602G>C (p.Thr534=) rs1592631034
NM_001370259.2(MEN1):c.1620C>T (p.Pro540=) rs928470958
NM_001370259.2(MEN1):c.1653C>T (p.Leu551=) rs1592630324
NM_001370259.2(MEN1):c.165T>C (p.Pro55=) rs1060503790
NM_001370259.2(MEN1):c.1740G>A (p.Thr580=) rs1114167530
NM_001370259.2(MEN1):c.225C>T (p.Leu75=) rs1333791405
NM_001370259.2(MEN1):c.228C>T (p.Thr76=) rs1394017906
NM_001370259.2(MEN1):c.252T>C (p.Ser84=) rs1592658989
NM_001370259.2(MEN1):c.390C>T (p.Ser130=) rs771272168
NM_001370259.2(MEN1):c.411G>C (p.Arg137=) rs371437505
NM_001370259.2(MEN1):c.446-10C>T rs1442401628
NM_001370259.2(MEN1):c.502C>T (p.Leu168=) rs1555165846
NM_001370259.2(MEN1):c.582T>G (p.Ala194=) rs1592650942
NM_001370259.2(MEN1):c.588C>T (p.Val196=) rs1592650906
NM_001370259.2(MEN1):c.630A>C (p.Thr210=) rs1592650685
NM_001370259.2(MEN1):c.639C>A (p.Ala213=) rs746067825
NM_001370259.2(MEN1):c.642T>C (p.Gly214=) rs931878410
NM_001370259.2(MEN1):c.64C>T (p.Leu22=) rs1592660695
NM_001370259.2(MEN1):c.667C>T (p.Leu223=) rs1592649487
NM_001370259.2(MEN1):c.741T>C (p.Ile247=) rs1592648877
NM_001370259.2(MEN1):c.79C>T (p.Leu27=) rs1006536599
NM_001370259.2(MEN1):c.81G>C (p.Leu27=) rs1592660553
NM_001370259.2(MEN1):c.824+9A>G rs774166628
NM_001370259.2(MEN1):c.900C>T (p.Thr300=) rs1592646297
NM_001370259.2(MEN1):c.903C>T (p.Leu301=) rs1592646283
NM_001370259.2(MEN1):c.906C>T (p.Tyr302=) rs1592646265
NM_001370259.2(MEN1):c.913-8C>T rs373893527
NM_001370259.2(MEN1):c.960C>G (p.Pro320=) rs1592643701
NM_130799.2(MEN1):c.-13_-7dup rs1217276136

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