ClinVar Miner

List of variants in gene MEN1 reported as likely pathogenic for Multiple endocrine neoplasia, type 1

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Total variants: 31
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HGVS dbSNP
NM_000244.3(MEN1):c.1028dupT (p.Gln344Alafs) rs386134245
NM_000244.3(MEN1):c.1064+2T>C rs1555164946
NM_000244.3(MEN1):c.1078delC (p.Arg360Glyfs) rs386134246
NM_000244.3(MEN1):c.1189dupG (p.Glu397Glyfs) rs386134247
NM_000244.3(MEN1):c.1277G>A (p.Cys426Tyr) rs386134249
NM_000244.3(MEN1):c.1326dup (p.Thr443Hisfs) rs1555164184
NM_000244.3(MEN1):c.1A>G (p.Met1Val) rs386134250
NM_000244.3(MEN1):c.252dupT (p.Ile85Tyrfs) rs386134253
NM_000244.3(MEN1):c.417C>G (p.His139Gln) rs386134254
NM_000244.3(MEN1):c.480_481insAATT (p.Gly161Asnfs) rs386134255
NM_000244.3(MEN1):c.664_669+2delGAGCGGGT rs386134258
NM_000244.3(MEN1):c.773C>A (p.Ser258Ter) rs386134259
NM_000244.3(MEN1):c.970dupT (p.Tyr324Leufs) rs386134261
NM_130799.2(MEN1):c.1117C>T (p.Pro373Ser)
NM_130799.2(MEN1):c.113C>T (p.Ser38Phe) rs794728616
NM_130799.2(MEN1):c.1328C>A (p.Ser443Tyr) rs1060499981
NM_130799.2(MEN1):c.1350+2T>C rs1555164115
NM_130799.2(MEN1):c.1351-1G>A rs794728629
NM_130799.2(MEN1):c.1351-1G>C rs794728629
NM_130799.2(MEN1):c.1351-2A>G rs1060499986
NM_130799.2(MEN1):c.1660C>T (p.Gln554Ter) rs794728631
NM_130799.2(MEN1):c.1664G>A (p.Ser555Asn) rs863224527
NM_130799.2(MEN1):c.1739delC (p.Thr580Argfs) rs864622617
NM_130799.2(MEN1):c.1A>T (p.Met1Leu) rs386134250
NM_130799.2(MEN1):c.35C>T (p.Pro12Leu) rs794728614
NM_130799.2(MEN1):c.3G>A (p.Met1Ile) rs786204242
NM_130799.2(MEN1):c.446-2A>G rs886042035
NM_130799.2(MEN1):c.526G>C (p.Ala176Pro) rs376872829
NM_130799.2(MEN1):c.762_768dup (p.Leu257Glyfs) rs1555165488
NM_130799.2(MEN1):c.851C>A (p.Ala284Glu)
NM_130799.2(MEN1):c.912+1G>C rs398124437

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