ClinVar Miner

List of variants in gene MEN1 reported as uncertain significance for not specified

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001370259.2(MEN1):c.-22C>A rs374749001 0.00073
NM_001370259.2(MEN1):c.*470A>G rs778272737 0.00048
NM_001370259.2(MEN1):c.1351-4C>T rs764408631 0.00014
NM_001370259.2(MEN1):c.1535C>T (p.Ser512Leu) rs141679530 0.00011
NM_001370259.2(MEN1):c.511C>T (p.Arg171Trp) rs143329068 0.00009
NM_001370259.2(MEN1):c.655-4del rs748005956 0.00009
NM_001370259.2(MEN1):c.563C>T (p.Pro188Leu) rs199706698 0.00005
NM_001370259.2(MEN1):c.1098A>T (p.Glu366Asp) rs149383809 0.00004
NM_001370259.2(MEN1):c.1522C>A (p.Gln508Lys) rs386833403 0.00002
NM_001370259.2(MEN1):c.1169C>T (p.Pro390Leu) rs761102084 0.00001
NM_001370259.2(MEN1):c.1567G>A (p.Ala523Thr) rs760683615 0.00001
NM_001370259.2(MEN1):c.189C>G (p.Phe63Leu) rs137880635 0.00001
NM_001370259.2(MEN1):c.635A>G (p.Asn212Ser) rs1438685841 0.00001
NM_001370259.2(MEN1):c.655-5C>G rs752563214 0.00001
NM_001370259.2(MEN1):c.-7_-1dup (p.Met1fs) rs758960344
NM_001370259.2(MEN1):c.119_124del (p.Val40_Leu41del) rs386134248
NM_001370259.2(MEN1):c.1295T>C (p.Leu432Pro) rs2136100876
NM_001370259.2(MEN1):c.1350G>C (p.Gln450His) rs1592636161
NM_001370259.2(MEN1):c.153C>A (p.Asn51Lys)
NM_001370259.2(MEN1):c.1643G>T (p.Gly548Val) rs2136081852
NM_001370259.2(MEN1):c.227C>T (p.Thr76Ile)
NM_001370259.2(MEN1):c.35C>G (p.Pro12Arg)
NM_001370259.2(MEN1):c.417C>A (p.His139Gln) rs386134254
NM_001370259.2(MEN1):c.638_639delinsAA (p.Ala213Glu) rs1114167518
NM_001370259.2(MEN1):c.644_652delinsGCCCCT (p.Val215_Arg218delinsGlyProTrp) rs386134257
NM_001370259.2(MEN1):c.652C>T (p.Arg218Trp) rs794728620
NM_001370259.2(MEN1):c.654+3A>T rs1064793168
NM_001370259.2(MEN1):c.655-5dup rs772016629
NM_001370259.2(MEN1):c.655-6C>A rs77461664
NM_001370259.2(MEN1):c.686G>A (p.Arg229His) rs878855197
NM_001370259.2(MEN1):c.689G>T (p.Cys230Phe)
NM_001370259.2(MEN1):c.776T>C (p.Leu259Pro) rs2136139920
NM_001370259.2(MEN1):c.784-19TC[2] rs764290037
NM_001370259.2(MEN1):c.830C>A (p.Pro277His) rs1060499973
NM_001370259.2(MEN1):c.869A>C (p.Glu290Ala) rs1213891703
NM_001370259.2(MEN1):c.897C>T (p.Leu299=) rs1409781409
NM_001370259.2(MEN1):c.913-65_913-14del rs1555165154
NM_001370259.2(MEN1):c.979T>G (p.Tyr327Asp) rs1259383083

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