ClinVar Miner

List of variants in gene IGHMBP2 reported as likely benign for not provided

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Total variants: 44
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HGVS dbSNP
NM_002180.2(IGHMBP2):c.103A>G (p.Ile35Val) rs199586231
NM_002180.2(IGHMBP2):c.1071C>T (p.Ala357=) rs755300047
NM_002180.2(IGHMBP2):c.1193C>T (p.Ala398Val) rs35193202
NM_002180.2(IGHMBP2):c.1236-6G>A rs201538340
NM_002180.2(IGHMBP2):c.1236-6G>C rs201538340
NM_002180.2(IGHMBP2):c.1596C>T (p.Ala532=) rs988590959
NM_002180.2(IGHMBP2):c.1737C>T (p.Phe579=) rs368775789
NM_002180.2(IGHMBP2):c.1757-149C>T rs58975356
NM_002180.2(IGHMBP2):c.2022G>A (p.Arg674=) rs111366439
NM_002180.2(IGHMBP2):c.2355G>A (p.Arg785=) rs147954772
NM_002180.2(IGHMBP2):c.2397C>T (p.Thr799=) rs763818374
NM_002180.2(IGHMBP2):c.257-279T>C rs142133560
NM_002180.2(IGHMBP2):c.2619G>A (p.Pro873=) rs373001247
NM_002180.2(IGHMBP2):c.2691C>T (p.Cys897=) rs146286133
NM_002180.2(IGHMBP2):c.2784+111C>A rs79957506
NM_002180.2(IGHMBP2):c.2837G>A (p.Arg946Gln) rs149824485
NM_002180.2(IGHMBP2):c.2856C>T (p.Ala952=) rs759627672
NM_002180.2(IGHMBP2):c.2976G>A (p.Gly992=) rs755792559
NM_002180.2(IGHMBP2):c.304G>T (p.Ala102Ser) rs35610053
NM_002180.2(IGHMBP2):c.548-223C>T rs149249976
NM_002180.2(IGHMBP2):c.861C>G (p.Ser287Arg) rs564645287
NM_002180.3(IGHMBP2):c.1038C>T (p.Asn346=) rs773013486
NM_002180.3(IGHMBP2):c.1077C>T (p.Gly359=) rs1247103419
NM_002180.3(IGHMBP2):c.1235+9C>T rs553889213
NM_002180.3(IGHMBP2):c.1395T>C (p.Ser465=) rs1594451498
NM_002180.3(IGHMBP2):c.1410C>T (p.His470=) rs1484199036
NM_002180.3(IGHMBP2):c.1452G>A (p.Thr484=) rs1368846781
NM_002180.3(IGHMBP2):c.1479C>G (p.Thr493=) rs370367228
NM_002180.3(IGHMBP2):c.1479C>T (p.Thr493=) rs370367228
NM_002180.3(IGHMBP2):c.1524G>T (p.Ser508=) rs747627986
NM_002180.3(IGHMBP2):c.1584T>G (p.Ala528=) rs1461885178
NM_002180.3(IGHMBP2):c.1722C>T (p.Ala574=) rs200081534
NM_002180.3(IGHMBP2):c.1757-6T>C rs1594455341
NM_002180.3(IGHMBP2):c.1851C>T (p.Val617=) rs780238088
NM_002180.3(IGHMBP2):c.2544C>T (p.Pro848=) rs746248057
NM_002180.3(IGHMBP2):c.2838G>A (p.Arg946=) rs778821393
NM_002180.3(IGHMBP2):c.2874C>T (p.Asn958=) rs779753312
NM_002180.3(IGHMBP2):c.2949G>A (p.Gln983=) rs761315649
NM_002180.3(IGHMBP2):c.555G>A (p.Leu185=) rs1176973229
NM_002180.3(IGHMBP2):c.585C>T (p.Ser195=) rs1442536361
NM_002180.3(IGHMBP2):c.597G>A (p.Ala199=) rs780961121
NM_002180.3(IGHMBP2):c.6C>T (p.Ala2=) rs1168042239
NM_002180.3(IGHMBP2):c.711+10G>C rs1484976321
NM_002180.3(IGHMBP2):c.861C>T (p.Ser287=) rs564645287

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