ClinVar Miner

List of variants reported as uncertain significance for obsolete accelerated tumor formation, susceptibility to by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_002392.6(MDM2):c.1232A>G (p.Tyr411Cys) rs367597251 0.00052
NM_002392.6(MDM2):c.961C>T (p.Leu321Phe) rs78419579 0.00024
NM_002392.6(MDM2):c.536A>G (p.Asp179Gly) rs138567205 0.00020
NM_002392.6(MDM2):c.44C>T (p.Pro15Leu) rs201821879 0.00019
NM_002392.6(MDM2):c.14+3A>G rs769890846 0.00008
NM_002392.6(MDM2):c.1242A>C (p.Gln414His) rs201686188 0.00006
NM_002392.6(MDM2):c.350A>G (p.Asn117Ser) rs767475639 0.00004
NM_002392.6(MDM2):c.1241A>T (p.Gln414Leu) rs201788800 0.00003
NM_002392.6(MDM2):c.1289A>T (p.Glu430Val) rs1286039833 0.00003
NM_002392.6(MDM2):c.818A>C (p.Glu273Ala) rs371801914 0.00003
NM_002392.6(MDM2):c.1121A>G (p.Asn374Ser) rs553794444 0.00002
NM_002392.6(MDM2):c.309G>A (p.Arg103=) rs766553126 0.00002
NM_002392.6(MDM2):c.995G>A (p.Arg332His) rs763077439 0.00002
NM_002392.6(MDM2):c.1039A>G (p.Ile347Val) rs768100456 0.00001
NM_002392.6(MDM2):c.1219A>G (p.Ser407Gly) rs570992498 0.00001
NM_002392.6(MDM2):c.1237A>G (p.Ser413Gly) rs780673045 0.00001
NM_002392.6(MDM2):c.212G>A (p.Arg71Gln) rs1385829631 0.00001
NM_002392.6(MDM2):c.226A>C (p.Lys76Gln) rs774100788 0.00001
NM_002392.6(MDM2):c.365C>T (p.Ser122Leu) rs567563488 0.00001
NM_002392.6(MDM2):c.46A>G (p.Thr16Ala) rs1450828029 0.00001
NM_002392.6(MDM2):c.57_59del (p.Val20del) rs1367482093 0.00001
NM_002392.6(MDM2):c.631A>C (p.Ile211Leu) rs750452466 0.00001
NM_002392.6(MDM2):c.683C>T (p.Pro228Leu) rs1387843274 0.00001
NM_002392.6(MDM2):c.886T>G (p.Ser296Ala) rs1286851604 0.00001
NM_002392.6(MDM2):c.913T>G (p.Leu305Val) rs547696481 0.00001
NM_002392.6(MDM2):c.918T>C (p.Ala306=) rs770653304 0.00001
NM_002392.6(MDM2):c.91G>C (p.Glu31Gln) rs1246173207 0.00001
NM_002392.6(MDM2):c.955C>A (p.Pro319Thr) rs577942747 0.00001
NC_000012.11:g.(?_69202258)_(69233629_?)dup
NM_002392.6(MDM2):c.1002T>A (p.Asn334Lys) rs199812774
NM_002392.6(MDM2):c.1030A>G (p.Lys344Glu)
NM_002392.6(MDM2):c.1079A>G (p.Glu360Gly)
NM_002392.6(MDM2):c.1103G>A (p.Cys368Tyr)
NM_002392.6(MDM2):c.1114A>G (p.Ile372Val)
NM_002392.6(MDM2):c.1150A>T (p.Asn384Tyr)
NM_002392.6(MDM2):c.1161A>C (p.Lys387Asn)
NM_002392.6(MDM2):c.1190G>A (p.Ser397Asn)
NM_002392.6(MDM2):c.1191T>G (p.Ser397Arg)
NM_002392.6(MDM2):c.1202C>G (p.Ser401Cys) rs1293117772
NM_002392.6(MDM2):c.1202C>T (p.Ser401Phe)
NM_002392.6(MDM2):c.1284_1287del (p.Glu429fs)
NM_002392.6(MDM2):c.1301C>G (p.Ser434Cys)
NM_002392.6(MDM2):c.1304G>A (p.Ser435Asn)
NM_002392.6(MDM2):c.1309C>T (p.Pro437Ser)
NM_002392.6(MDM2):c.14+5T>G
NM_002392.6(MDM2):c.1405A>T (p.Thr469Ser)
NM_002392.6(MDM2):c.1446A>G (p.Pro482=) rs1883605122
NM_002392.6(MDM2):c.15-2A>G rs2136105482
NM_002392.6(MDM2):c.154G>C (p.Asp52His) rs2136114145
NM_002392.6(MDM2):c.174+18A>G
NM_002392.6(MDM2):c.178C>G (p.Leu60Val)
NM_002392.6(MDM2):c.185A>T (p.Tyr62Phe) rs2136121383
NM_002392.6(MDM2):c.305A>G (p.His102Arg)
NM_002392.6(MDM2):c.377C>T (p.Thr126Ile)
NM_002392.6(MDM2):c.385A>C (p.Ser129Arg)
NM_002392.6(MDM2):c.398G>A (p.Cys133Tyr)
NM_002392.6(MDM2):c.403C>T (p.Leu135Phe)
NM_002392.6(MDM2):c.421C>G (p.Gln141Glu)
NM_002392.6(MDM2):c.431T>C (p.Leu144Pro)
NM_002392.6(MDM2):c.443T>C (p.Leu148Pro)
NM_002392.6(MDM2):c.50A>G (p.Asp17Gly)
NM_002392.6(MDM2):c.523+5A>G rs1423747454
NM_002392.6(MDM2):c.524-2A>G
NM_002392.6(MDM2):c.560G>C (p.Arg187Thr) rs776774609
NM_002392.6(MDM2):c.565C>T (p.Arg189Cys) rs1555187172
NM_002392.6(MDM2):c.56C>T (p.Ala19Val)
NM_002392.6(MDM2):c.582T>A (p.Ser194Arg)
NM_002392.6(MDM2):c.583A>G (p.Ile195Val) rs1241409542
NM_002392.6(MDM2):c.589C>T (p.Leu197Phe)
NM_002392.6(MDM2):c.613C>G (p.Leu205Val)
NM_002392.6(MDM2):c.643A>G (p.Arg215Gly)
NM_002392.6(MDM2):c.652A>G (p.Ser218Gly)
NM_002392.6(MDM2):c.694G>T (p.Ala232Ser)
NM_002392.6(MDM2):c.698_700del (p.Gly233del) rs763055876
NM_002392.6(MDM2):c.815A>G (p.Gln272Arg)
NM_002392.6(MDM2):c.85G>A (p.Glu29Lys) rs1361311287
NM_002392.6(MDM2):c.88C>A (p.Gln30Lys)
NM_002392.6(MDM2):c.910T>C (p.Ser304Pro)
NM_002392.6(MDM2):c.948A>C (p.Glu316Asp) rs778582378
NM_002392.6(MDM2):c.971A>T (p.His324Leu) rs2136177157
NM_002392.6(MDM2):c.980G>C (p.Arg327Thr)
NM_002392.6(MDM2):c.992T>G (p.Leu331Arg)
NM_002392.6(MDM2):c.999G>T (p.Glu333Asp)

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