ClinVar Miner

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

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Total variants: 27
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HGVS dbSNP
NM_000244.3(MEN1):c.1028T>C (p.Leu343Pro) rs1114167480
NM_000244.3(MEN1):c.1079G>A (p.Arg360Gln) rs1114167474
NM_000244.3(MEN1):c.1132C>G (p.Pro378Ala) rs794728627
NM_000244.3(MEN1):c.1189del (p.Glu397fs) rs386134247
NM_000244.3(MEN1):c.125G>T (p.Gly42Val) rs1565652689
NM_000244.3(MEN1):c.1277G>A (p.Cys426Tyr) rs386134249
NM_000244.3(MEN1):c.1617_1633del (p.Ala540fs) rs794728660
NM_000244.3(MEN1):c.1682_1684AGA[1] (p.Lys562del) rs794728661
NM_000244.3(MEN1):c.168del (p.Asn57fs) rs1060499990
NM_000244.3(MEN1):c.1745T>C (p.Leu582Pro) rs794728634
NM_000244.3(MEN1):c.1A>G (p.Met1Val) rs386134250
NM_000244.3(MEN1):c.266_286del (p.Leu89_Ala95del) rs1064792906
NM_000244.3(MEN1):c.481G>C (p.Gly161Arg) rs1085307471
NM_000244.3(MEN1):c.482G>A (p.Gly161Asp) rs794728648
NM_000244.3(MEN1):c.530A>T (p.Asp177Val) rs794728618
NM_000244.3(MEN1):c.541G>C (p.Ala181Pro) rs376872829
NM_000244.3(MEN1):c.550G>A (p.Glu184Lys) rs1064793167
NM_000244.3(MEN1):c.65T>G (p.Leu22Arg) rs104894256
NM_000244.3(MEN1):c.673T>C (p.Trp225Arg) rs1085307971
NM_000244.3(MEN1):c.688G>A (p.Gly230Arg) rs1057521110
NM_000244.3(MEN1):c.699del (p.Met233fs) rs1064795635
NM_000244.3(MEN1):c.703T>C (p.Cys235Arg) rs1555165570
NM_000244.3(MEN1):c.76G>A (p.Glu26Lys) rs28931612
NM_000244.3(MEN1):c.788_790dup (p.Gln263dup) rs1057517760
NM_000244.3(MEN1):c.798+2T>G rs1057524571
NM_000244.3(MEN1):c.839+5G>A rs1064793398
NM_000244.3(MEN1):c.937T>C (p.Ser313Pro) rs1064793169

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