Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.64803514_64804816delCA891843125MEN1c.1351_*820del (n.[c.1351_*820del;Val451=])
c.1366_*820del (n.[c.1366_*820del;Val456=])
c.1186_*820del (n.[c.1186_*820del;Val396Ter])
 ClinVar
11g.64804201_64804818delinsCGGGACCGGGAACCTAGGGTTTGGGTAGAGGTGAGGCCTGTCCCCTTTGGGCTGGGGGCAGAACATGGGCTCAGAGTTGGGGGACTAAGGGCGGAGCCTGGGTCCCCACAAGCGGTCCGAAGTCCCCAGTAGTTCAGAGGCCTTTGCGCTGCCGCTTGAGGAAAGACAGAGTGTAGTCACTAGGGGTGGACACTTTCTGCTTCTTCATCTGCACTTGCGACTGTGCCGTGAGTTGCAGCTTGATGGCGCTCGAGTTGATCTTGGTGGCCACCAGCAGCTCCTTCATGCCCTTCATCTTCTCACTCTGGAAAGTGAGCACTGGACCCTCCGGCGGTGGTGATGCTGTGGGTGCTGGCACCTGAGCCGTGCTGCCACCTTCAGGGCCTCGGGCTGTGCCAGCGACAGTCCCAGGAGGCTTCCGGGGGGGTCCTGACACTGCACCCTGGCCGGTGCCCAGGCCCTTGTCCAGTGCTGGCTTCTTGGGCGGCGGGGGCTCCTCTGGCTTGGACTCCCGCCGTGGGCCCCGCCGCCGGCCTTCCCGGGCTTCCTCGCCCCACGGCTCCTCGGCCTCGGCCGCCTCGGCCTCTCGGCTCACTATGCGCACCTTCTGCCGCACCTCA1978916146MEN1c.1366-2_*133delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.*659-2_*1274delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.1351-11_*133delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.1351-2_*133delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.*447-2_*1062delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.702-11_1308delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
n.1844-2_2459delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
n.1313-2_1928delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
n.1852-2_2467delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
n.1628-2_2243delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.1477-2_*133delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.1186-2_*133delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.1246-2_*133delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
c.1492-2_*133delinsAGGTGCGGCAGAAGGTGCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGGAAGGCCGGCGGCGGGGCCCACGGCGGGAGTCCAAGCCAGAGGAGCCCCCGCCGCCCAAGAAGCCAGCACTGGACAAGGGCCTGGGCACCGGCCAGGGTGCAGTGTCAGGACCCCCCCGGAAGCCTCCTGGGACTGTCGCTGGCACAGCCCGAGGCCCTGAAGGTGGCAGCACGGCTCAGGTGCCAGCACCCACAGCATCACCACCGCCGGAGGGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCCATCAAGCTGCAACTCACGGCACAGTCGCAAGTGCAGATGAAGAAGCAGAAAGTGTCCACCCCTAGTGACTACACTCTGTCTTTCCTCAAGCGGCAGCGCAAAGGCCTCTGAACTACTGGGGACTTCGGACCGCTTGTGGGGACCCAGGCTCCGCCCTTAGTCCCCCAACTCTGAGCCCATGTTCTGCCCCCAGCCCAAAGGGGACAGGCCTCACCTCTACCCAAACCCTAGGTTCCCGGTCCCG
11g.64804205_64804821delCA891843126MEN1c.1366-2_*132del
c.*659-2_*1273del
c.1351-11_*132del
c.1351-2_*132del
c.*447-2_*1061del
c.702-11_1307del
n.1844-2_2458del
n.1313-2_1927del
n.1852-2_2466del
n.1628-2_2242del
c.1477-2_*132del
c.1186-2_*132del
c.1246-2_*132del
c.1492-2_*132del
 ClinVar dbSNP
11g.64804445_64804524delinsGGCGCTCGAGTTGATCTTGGTGGCCACCAGCAGCTCCTTCATGCCCTTCATCTTCTCACTCTGGAAAGTGAGCACTGGACCA1978916904MEN1c.1658_1737delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (p.Gly553=)
c.*951_*1030delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (n.*951_*1030delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC)
c.1634_1713delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (p.Gly545=)
c.1643_1722delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (p.Gly548=)
c.*739_*818delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (n.*739_*818delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC)
c.985_1064delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC
n.2136_2215delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC
n.1605_1684delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC
n.2144_2223delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC
n.1920_1999delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC
c.1769_1848delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (p.Gly590=)
c.1478_1557delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (p.Gly493=)
c.1538_1617delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (p.Gly513=)
n.1192_1271delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC
c.1784_1863delinsGTCCAGTGCTCACTTTCCAGAGTGAGAAGATGAAGGGCATGAAGGAGCTGCTGGTGGCCACCAAGATCAACTCGAGCGCC (p.Gly595=)
11g.64804446_64804524delinsCACA645369564MEN1c.1658_1736delinsTG (p.Gly553ValfsTer23)
c.*951_*1029delinsTG (n.*951_*1029delinsTG)
c.1634_1712delinsTG (p.Gly545ValfsTer23)
c.1643_1721delinsTG (p.Gly548ValfsTer23)
c.*739_*817delinsTG (n.*739_*817delinsTG)
c.985_1063delinsTG
n.2136_2214delinsTG
n.1605_1683delinsTG
n.2144_2222delinsTG
n.1920_1998delinsTG
c.1769_1847delinsTG (p.Gly590ValfsTer23)
c.1478_1556delinsTG (p.Gly493ValfsTer23)
c.1538_1616delinsTG (p.Gly513ValfsTer23)
n.1192_1270delinsTG
c.1784_1862delinsTG (p.Gly595ValfsTer23)
 ClinVar dbSNP
11g.64804487_64804495delinsGCCCTTCATCA1978917182MEN1c.1687_1695delinsATGAAGGGC (p.Met563=)
c.*980_*988delinsATGAAGGGC (n.*980_*988delinsATGAAGGGC)
c.1663_1671delinsATGAAGGGC (p.Met555=)
c.1672_1680delinsATGAAGGGC (p.Met558=)
c.*768_*776delinsATGAAGGGC (n.*768_*776delinsATGAAGGGC)
c.1014_1022delinsATGAAGGGC
n.2165_2173delinsATGAAGGGC
n.1634_1642delinsATGAAGGGC
n.2173_2181delinsATGAAGGGC
n.1949_1957delinsATGAAGGGC
c.1798_1806delinsATGAAGGGC (p.Met600=)
c.1507_1515delinsATGAAGGGC (p.Met503=)
c.1567_1575delinsATGAAGGGC (p.Met523=)
n.1221_1229delinsATGAAGGGC
c.1813_1821delinsATGAAGGGC (p.Met605=)
11g.64804489_64804496delCA916081642MEN1c.1687_1694del (p.Met563HisfsTer?)
c.*980_*987del (n.*980_*987del)
c.1663_1670del (p.Met555HisfsTer?)
c.1672_1679del (p.Met558HisfsTer?)
c.*768_*775del (n.*768_*775del)
c.1014_1021del
n.2165_2172del
n.1634_1641del
n.2173_2180del
n.1949_1956del
c.1798_1805del (p.Met600HisfsTer?)
c.1507_1514del (p.Met503HisfsTer?)
c.1567_1574del (p.Met523HisfsTer?)
n.1221_1228del
c.1813_1820del (p.Met605HisfsTer?)
 ClinVar dbSNP
11g.64804494_64804496delCA2580084411MEN1c.1688_1690del (p.Met563del)
c.*981_*983del (n.*981_*983del)
c.1664_1666del (p.Met555del)
c.1673_1675del (p.Met558del)
c.*769_*771del (n.*769_*771del)
c.1015_1017del
n.2166_2168del
n.1635_1637del
n.2055_2057del
n.2174_2176del
n.1950_1952del
c.1799_1801del (p.Met600del)
c.1508_1510del (p.Met503del)
c.1568_1570del (p.Met523del)
n.1222_1224del
c.1814_1816del (p.Met605del)
 ClinVar
11g.64804493C>ACA381177745MEN1c.1689G>T (p.Met563Ile)
c.*982G>T (n.*982G>T)
c.1665G>T (p.Met555Ile)
c.1674G>T (p.Met558Ile)
c.*770G>T (n.*770G>T)
c.1016G>T
n.2167G>T
n.1636G>T
n.2056G>T
n.2175G>T
n.1951G>T
c.1800G>T (p.Met600Ile)
c.1509G>T (p.Met503Ile)
c.1569G>T (p.Met523Ile)
n.1223G>T
c.1815G>T (p.Met605Ile)
 dbSNP
11g.64804493C>GCA381177750MEN1c.1689G>C (p.Met563Ile)
c.*982G>C (n.*982G>C)
c.1665G>C (p.Met555Ile)
c.1674G>C (p.Met558Ile)
c.*770G>C (n.*770G>C)
c.1016G>C
n.2167G>C
n.1636G>C
n.2056G>C
n.2175G>C
n.1951G>C
c.1800G>C (p.Met600Ile)
c.1509G>C (p.Met503Ile)
c.1569G>C (p.Met523Ile)
n.1223G>C
c.1815G>C (p.Met605Ile)
11g.64804493C>TCA381177751MEN1c.1689G>A (p.Met563Ile)
c.*982G>A (n.*982G>A)
c.1665G>A (p.Met555Ile)
c.1674G>A (p.Met558Ile)
c.*770G>A (n.*770G>A)
c.1016G>A
n.2167G>A
n.1636G>A
n.2056G>A
n.2175G>A
n.1951G>A
c.1800G>A (p.Met600Ile)
c.1509G>A (p.Met503Ile)
c.1569G>A (p.Met523Ile)
n.1223G>A
c.1815G>A (p.Met605Ile)
 ClinVar dbSNP
11g.64804493dupCA891843127MEN1c.1689dup (p.Lys564GlufsTer?)
c.*982dup (n.*982dup)
c.1665dup (p.Lys556GlufsTer?)
c.1674dup (p.Lys559GlufsTer?)
c.*770dup (n.*770dup)
c.1016dup
n.2167dup
n.1636dup
n.2056dup
n.2175dup
n.1951dup
c.1800dup (p.Lys601GlufsTer?)
c.1509dup (p.Lys504GlufsTer?)
c.1569dup (p.Lys524GlufsTer?)
n.1223dup
c.1815dup (p.Lys606GlufsTer?)
 ClinVar dbSNP
11g.64804494A>CCA381177753MEN1c.1688T>G (p.Met563Arg)
c.*981T>G (n.*981T>G)
c.1664T>G (p.Met555Arg)
c.1673T>G (p.Met558Arg)
c.*769T>G (n.*769T>G)
c.1015T>G
n.2166T>G
n.1635T>G
n.2055T>G
n.2174T>G
n.1950T>G
c.1799T>G (p.Met600Arg)
c.1508T>G (p.Met503Arg)
c.1568T>G (p.Met523Arg)
n.1222T>G
c.1814T>G (p.Met605Arg)
11g.64804494A>GCA381177754MEN1c.1688T>C (p.Met563Thr)
c.*981T>C (n.*981T>C)
c.1664T>C (p.Met555Thr)
c.1673T>C (p.Met558Thr)
c.*769T>C (n.*769T>C)
c.1015T>C
n.2166T>C
n.1635T>C
n.2055T>C
n.2174T>C
n.1950T>C
c.1799T>C (p.Met600Thr)
c.1508T>C (p.Met503Thr)
c.1568T>C (p.Met523Thr)
n.1222T>C
c.1814T>C (p.Met605Thr)
 ClinVar
11g.64804494A>TCA381177756MEN1c.1688T>A (p.Met563Lys)
c.*981T>A (n.*981T>A)
c.1664T>A (p.Met555Lys)
c.1673T>A (p.Met558Lys)
c.*769T>A (n.*769T>A)
c.1015T>A
n.2166T>A
n.1635T>A
n.2055T>A
n.2174T>A
n.1950T>A
c.1799T>A (p.Met600Lys)
c.1508T>A (p.Met503Lys)
c.1568T>A (p.Met523Lys)
n.1222T>A
c.1814T>A (p.Met605Lys)
11g.64804494_64804497delinsATCTCA1978917196MEN1c.1685_1688delinsAGAT (p.Lys562=)
c.*978_*981delinsAGAT (n.*978_*981delinsAGAT)
c.1661_1664delinsAGAT (p.Lys554=)
c.1670_1673delinsAGAT (p.Lys557=)
c.*766_*769delinsAGAT (n.*766_*769delinsAGAT)
c.1012_1015delinsAGAT
n.2163_2166delinsAGAT
n.1632_1635delinsAGAT
n.2052_2055delinsAGAT
n.2171_2174delinsAGAT
n.1947_1950delinsAGAT
c.1796_1799delinsAGAT (p.Lys599=)
c.1505_1508delinsAGAT (p.Lys502=)
c.1565_1568delinsAGAT (p.Lys522=)
n.1219_1222delinsAGAT
c.1811_1814delinsAGAT (p.Lys604=)
11g.64804494_64804525delinsGGCA2580084412MEN1c.1657_1688delinsCC (p.Gly553_Met563delinsPro)
c.*950_*981delinsCC (n.*950_*981delinsCC)
c.1633_1664delinsCC (p.Gly545_Met555delinsPro)
c.1642_1673delinsCC (p.Gly548_Met558delinsPro)
c.*738_*769delinsCC (n.*738_*769delinsCC)
c.984_1015delinsCC
n.2135_2166delinsCC
n.1604_1635delinsCC
n.2024_2055delinsCC
n.2143_2174delinsCC
n.1919_1950delinsCC
c.1768_1799delinsCC (p.Gly590_Met600delinsPro)
c.1477_1508delinsCC (p.Gly493_Met503delinsPro)
c.1537_1568delinsCC (p.Gly513_Met523delinsPro)
n.1191_1222delinsCC
c.1783_1814delinsCC (p.Gly595_Met605delinsPro)
 ClinVar
11g.64804495delCA2695214500MEN1c.1687del (p.Met563Ter)
c.*980del (n.*980del)
c.1663del (p.Met555Ter)
c.1672del (p.Met558Ter)
c.*768del (n.*768del)
c.1014del
n.2165del
n.1634del
n.2054del
n.2173del
n.1949del
c.1798del (p.Met600Ter)
c.1507del (p.Met503Ter)
c.1567del (p.Met523Ter)
n.1221del
c.1813del (p.Met605Ter)
11g.64804495T>ACA381177764MEN1c.1687A>T (p.Met563Leu)
c.*980A>T (n.*980A>T)
c.1663A>T (p.Met555Leu)
c.1672A>T (p.Met558Leu)
c.*768A>T (n.*768A>T)
c.1014A>T
n.2165A>T
n.1634A>T
n.2054A>T
n.2173A>T
n.1949A>T
c.1798A>T (p.Met600Leu)
c.1507A>T (p.Met503Leu)
c.1567A>T (p.Met523Leu)
n.1221A>T
c.1813A>T (p.Met605Leu)
11g.64804495T>CCA381177762MEN1c.1687A>G (p.Met563Val)
c.*980A>G (n.*980A>G)
c.1663A>G (p.Met555Val)
c.1672A>G (p.Met558Val)
c.*768A>G (n.*768A>G)
c.1014A>G
n.2165A>G
n.1634A>G
n.2054A>G
n.2173A>G
n.1949A>G
c.1798A>G (p.Met600Val)
c.1507A>G (p.Met503Val)
c.1567A>G (p.Met523Val)
n.1221A>G
c.1813A>G (p.Met605Val)
11g.64804495T>GCA381177759MEN1c.1687A>C (p.Met563Leu)
c.*980A>C (n.*980A>C)
c.1663A>C (p.Met555Leu)
c.1672A>C (p.Met558Leu)
c.*768A>C (n.*768A>C)
c.1014A>C
n.2165A>C
n.1634A>C
n.2054A>C
n.2173A>C
n.1949A>C
c.1798A>C (p.Met600Leu)
c.1507A>C (p.Met503Leu)
c.1567A>C (p.Met523Leu)
n.1221A>C
c.1813A>C (p.Met605Leu)
11g.64804498_64804500delCA009279MEN1c.1685_1687del (p.Lys562del)
c.*978_*980del (n.*978_*980del)
c.1661_1663del (p.Lys554del)
c.1670_1672del (p.Lys557del)
c.*766_*768del (n.*766_*768del)
c.1012_1014del
n.2163_2165del
n.1632_1634del
n.2052_2054del
n.2171_2173del
n.1947_1949del
c.1796_1798del (p.Lys599del)
c.1505_1507del (p.Lys502del)
c.1565_1567del (p.Lys522del)
n.1219_1221del
c.1811_1813del (p.Lys604del)
 ClinVar dbSNP
11g.64804496C>ACA381177766MEN1c.1686G>T (p.Lys562Asn)
c.*979G>T (n.*979G>T)
c.1662G>T (p.Lys554Asn)
c.1671G>T (p.Lys557Asn)
c.*767G>T (n.*767G>T)
c.1013G>T
n.2164G>T
n.1633G>T
n.2053G>T
n.2172G>T
n.1948G>T
c.1797G>T (p.Lys599Asn)
c.1506G>T (p.Lys502Asn)
c.1566G>T (p.Lys522Asn)
n.1220G>T
c.1812G>T (p.Lys604Asn)
 dbSNP
11g.64804496C>GCA381177768MEN1c.1686G>C (p.Lys562Asn)
c.*979G>C (n.*979G>C)
c.1662G>C (p.Lys554Asn)
c.1671G>C (p.Lys557Asn)
c.*767G>C (n.*767G>C)
c.1013G>C
n.2164G>C
n.1633G>C
n.2053G>C
n.2172G>C
n.1948G>C
c.1797G>C (p.Lys599Asn)
c.1506G>C (p.Lys502Asn)
c.1566G>C (p.Lys522Asn)
n.1220G>C
c.1812G>C (p.Lys604Asn)
11g.64804496C>TCA475163436MEN1c.1686G>A (p.Lys562=)
c.*979G>A (n.*979G>A)
c.1662G>A (p.Lys554=)
c.1671G>A (p.Lys557=)
c.*767G>A (n.*767G>A)
c.1013G>A
n.2164G>A
n.1633G>A
n.2053G>A
n.2172G>A
n.1948G>A
c.1797G>A (p.Lys599=)
c.1506G>A (p.Lys502=)
c.1566G>A (p.Lys522=)
n.1220G>A
c.1812G>A (p.Lys604=)
 gnomAD v4
11g.64804496_64804497delinsCTCA1978917207MEN1c.1685_1686delinsAG (p.Lys562=)
c.*978_*979delinsAG (n.*978_*979delinsAG)
c.1661_1662delinsAG (p.Lys554=)
c.1670_1671delinsAG (p.Lys557=)
c.*766_*767delinsAG (n.*766_*767delinsAG)
c.1012_1013delinsAG
n.2163_2164delinsAG
n.1632_1633delinsAG
n.2052_2053delinsAG
n.2171_2172delinsAG
n.1947_1948delinsAG
c.1796_1797delinsAG (p.Lys599=)
c.1505_1506delinsAG (p.Lys502=)
c.1565_1566delinsAG (p.Lys522=)
n.1219_1220delinsAG
c.1811_1812delinsAG (p.Lys604=)
11g.64804497T>ACA381177770MEN1c.1685A>T (p.Lys562Met)
c.*978A>T (n.*978A>T)
c.1661A>T (p.Lys554Met)
c.1670A>T (p.Lys557Met)
c.*766A>T (n.*766A>T)
c.1012A>T
n.2163A>T
n.1632A>T
n.2052A>T
n.2171A>T
n.1947A>T
c.1796A>T (p.Lys599Met)
c.1505A>T (p.Lys502Met)
c.1565A>T (p.Lys522Met)
n.1219A>T
c.1811A>T (p.Lys604Met)
 ClinVar
11g.64804497T>CCA381177772MEN1c.1685A>G (p.Lys562Arg)
c.*978A>G (n.*978A>G)
c.1661A>G (p.Lys554Arg)
c.1670A>G (p.Lys557Arg)
c.*766A>G (n.*766A>G)
c.1012A>G
n.2163A>G
n.1632A>G
n.2052A>G
n.2171A>G
n.1947A>G
c.1796A>G (p.Lys599Arg)
c.1505A>G (p.Lys502Arg)
c.1565A>G (p.Lys522Arg)
n.1219A>G
c.1811A>G (p.Lys604Arg)
11g.64804497T>GCA381177774MEN1c.1685A>C (p.Lys562Thr)
c.*978A>C (n.*978A>C)
c.1661A>C (p.Lys554Thr)
c.1670A>C (p.Lys557Thr)
c.*766A>C (n.*766A>C)
c.1012A>C
n.2163A>C
n.1632A>C
n.2052A>C
n.2171A>C
n.1947A>C
c.1796A>C (p.Lys599Thr)
c.1505A>C (p.Lys502Thr)
c.1565A>C (p.Lys522Thr)
n.1219A>C
c.1811A>C (p.Lys604Thr)
11g.64804498delCA915948596MEN1c.1685del (p.Lys562ArgfsTer2)
c.*978del (n.*978del)
c.1661del (p.Lys554ArgfsTer2)
c.1670del (p.Lys557ArgfsTer2)
c.*766del (n.*766del)
c.1012del
n.2163del
n.1632del
n.2052del
n.2171del
n.1947del
c.1796del (p.Lys599ArgfsTer2)
c.1505del (p.Lys502ArgfsTer2)
c.1565del (p.Lys522ArgfsTer2)
n.1219del
c.1811del (p.Lys604ArgfsTer2)
 ClinVar dbSNP
11g.64804498T>ACA381177780MEN1c.1684A>T (p.Lys562Ter)
c.*977A>T (n.*977A>T)
c.1660A>T (p.Lys554Ter)
c.1669A>T (p.Lys557Ter)
c.*765A>T (n.*765A>T)
c.1011A>T
n.2162A>T
n.1631A>T
n.2051A>T
n.2170A>T
n.1946A>T
c.1795A>T (p.Lys599Ter)
c.1504A>T (p.Lys502Ter)
c.1564A>T (p.Lys522Ter)
n.1218A>T
c.1810A>T (p.Lys604Ter)
11g.64804498T>CCA381177776MEN1c.1684A>G (p.Lys562Glu)
c.*977A>G (n.*977A>G)
c.1660A>G (p.Lys554Glu)
c.1669A>G (p.Lys557Glu)
c.*765A>G (n.*765A>G)
c.1011A>G
n.2162A>G
n.1631A>G
n.2051A>G
n.2170A>G
n.1946A>G
c.1795A>G (p.Lys599Glu)
c.1504A>G (p.Lys502Glu)
c.1564A>G (p.Lys522Glu)
n.1218A>G
c.1810A>G (p.Lys604Glu)
 ClinVar dbSNP
11g.64804498T>GCA381177778MEN1c.1684A>C (p.Lys562Gln)
c.*977A>C (n.*977A>C)
c.1660A>C (p.Lys554Gln)
c.1669A>C (p.Lys557Gln)
c.*765A>C (n.*765A>C)
c.1011A>C
n.2162A>C
n.1631A>C
n.2051A>C
n.2170A>C
n.1946A>C
c.1795A>C (p.Lys599Gln)
c.1504A>C (p.Lys502Gln)
c.1564A>C (p.Lys522Gln)
n.1218A>C
c.1810A>C (p.Lys604Gln)
11g.64804498T=CA1978917226MEN1c.1684A= (p.Lys562=)
c.*977A= (n.*977A=)
c.1660A= (p.Lys554=)
c.1669A= (p.Lys557=)
c.*765A= (n.*765A=)
c.1011A=
n.2162A=
n.1631A=
n.2051A=
n.2170A=
n.1946A=
c.1795A= (p.Lys599=)
c.1504A= (p.Lys502=)
c.1564A= (p.Lys522=)
n.1218A=
c.1810A= (p.Lys604=)
11g.64804498_64804502delinsTCTCACA1978917222MEN1c.1680_1684delinsTGAGA (p.Ser560=)
c.*973_*977delinsTGAGA (n.*973_*977delinsTGAGA)
c.1656_1660delinsTGAGA (p.Ser552=)
c.1665_1669delinsTGAGA (p.Ser555=)
c.*761_*765delinsTGAGA (n.*761_*765delinsTGAGA)
c.1007_1011delinsTGAGA
n.2158_2162delinsTGAGA
n.1627_1631delinsTGAGA
n.2047_2051delinsTGAGA
n.2166_2170delinsTGAGA
n.1942_1946delinsTGAGA
c.1791_1795delinsTGAGA (p.Ser597=)
c.1500_1504delinsTGAGA (p.Ser500=)
c.1560_1564delinsTGAGA (p.Ser520=)
n.1214_1218delinsTGAGA
c.1806_1810delinsTGAGA (p.Ser602=)
11g.64804499_64804506dupCA2695214501MEN1c.1677_1684dup (p.Lys562ArgfsTer5)
c.*970_*977dup (n.*970_*977dup)
c.1653_1660dup (p.Lys554ArgfsTer5)
c.1662_1669dup (p.Lys557ArgfsTer5)
c.*758_*765dup (n.*758_*765dup)
c.1004_1011dup
n.2155_2162dup
n.1624_1631dup
n.2044_2051dup
n.2163_2170dup
n.1939_1946dup
c.1788_1795dup (p.Lys599ArgfsTer5)
c.1497_1504dup (p.Lys502ArgfsTer5)
c.1557_1564dup (p.Lys522ArgfsTer5)
n.1211_1218dup
c.1803_1810dup (p.Lys604ArgfsTer5)
11g.64804499C>ACA381177781MEN1c.1683G>T (p.Glu561Asp)
c.*976G>T (n.*976G>T)
c.1659G>T (p.Glu553Asp)
c.1668G>T (p.Glu556Asp)
c.*764G>T (n.*764G>T)
c.1010G>T
n.2161G>T
n.1630G>T
n.2050G>T
n.2169G>T
n.1945G>T
c.1794G>T (p.Glu598Asp)
c.1503G>T (p.Glu501Asp)
c.1563G>T (p.Glu521Asp)
n.1217G>T
c.1809G>T (p.Glu603Asp)
11g.64804499C>GCA381177783MEN1c.1683G>C (p.Glu561Asp)
c.*976G>C (n.*976G>C)
c.1659G>C (p.Glu553Asp)
c.1668G>C (p.Glu556Asp)
c.*764G>C (n.*764G>C)
c.1010G>C
n.2161G>C
n.1630G>C
n.2050G>C
n.2169G>C
n.1945G>C
c.1794G>C (p.Glu598Asp)
c.1503G>C (p.Glu501Asp)
c.1563G>C (p.Glu521Asp)
n.1217G>C
c.1809G>C (p.Glu603Asp)
11g.64804499C>TCA475163451MEN1c.1683G>A (p.Glu561=)
c.*976G>A (n.*976G>A)
c.1659G>A (p.Glu553=)
c.1668G>A (p.Glu556=)
c.*764G>A (n.*764G>A)
c.1010G>A
n.2161G>A
n.1630G>A
n.2050G>A
n.2169G>A
n.1945G>A
c.1794G>A (p.Glu598=)
c.1503G>A (p.Glu501=)
c.1563G>A (p.Glu521=)
n.1217G>A
c.1809G>A (p.Glu603=)
 ClinVar dbSNP
11g.64804502_64804505delCA645369569MEN1c.1680_1683del (p.Ser560ArgfsTer3)
c.*973_*976del (n.*973_*976del)
c.1656_1659del (p.Ser552ArgfsTer3)
c.1665_1668del (p.Ser555ArgfsTer3)
c.*761_*764del (n.*761_*764del)
c.1007_1010del
n.2158_2161del
n.1627_1630del
n.2047_2050del
n.2166_2169del
n.1942_1945del
c.1791_1794del (p.Ser597ArgfsTer3)
c.1500_1503del (p.Ser500ArgfsTer3)
c.1560_1563del (p.Ser520ArgfsTer3)
n.1214_1217del
c.1806_1809del (p.Ser602ArgfsTer3)
 ClinVar dbSNP gnomAD v4
11g.64804500T>ACA381177786MEN1c.1682A>T (p.Glu561Val)
c.*975A>T (n.*975A>T)
c.1658A>T (p.Glu553Val)
c.1667A>T (p.Glu556Val)
c.*763A>T (n.*763A>T)
c.1009A>T
n.2160A>T
n.1629A>T
n.2049A>T
n.2168A>T
n.1944A>T
c.1793A>T (p.Glu598Val)
c.1502A>T (p.Glu501Val)
c.1562A>T (p.Glu521Val)
n.1216A>T
c.1808A>T (p.Glu603Val)
11g.64804500T>CCA381177787MEN1c.1682A>G (p.Glu561Gly)
c.*975A>G (n.*975A>G)
c.1658A>G (p.Glu553Gly)
c.1667A>G (p.Glu556Gly)
c.*763A>G (n.*763A>G)
c.1009A>G
n.2160A>G
n.1629A>G
n.2049A>G
n.2168A>G
n.1944A>G
c.1793A>G (p.Glu598Gly)
c.1502A>G (p.Glu501Gly)
c.1562A>G (p.Glu521Gly)
n.1216A>G
c.1808A>G (p.Glu603Gly)
11g.64804500T>GCA381177788MEN1c.1682A>C (p.Glu561Ala)
c.*975A>C (n.*975A>C)
c.1658A>C (p.Glu553Ala)
c.1667A>C (p.Glu556Ala)
c.*763A>C (n.*763A>C)
c.1009A>C
n.2160A>C
n.1629A>C
n.2049A>C
n.2168A>C
n.1944A>C
c.1793A>C (p.Glu598Ala)
c.1502A>C (p.Glu501Ala)
c.1562A>C (p.Glu521Ala)
n.1216A>C
c.1808A>C (p.Glu603Ala)
11g.64804501C>ACA381177791MEN1c.1681G>T (p.Glu561Ter)
c.*974G>T (n.*974G>T)
c.1657G>T (p.Glu553Ter)
c.1666G>T (p.Glu556Ter)
c.*762G>T (n.*762G>T)
c.1008G>T
n.2159G>T
n.1628G>T
n.2048G>T
n.2167G>T
n.1943G>T
c.1792G>T (p.Glu598Ter)
c.1501G>T (p.Glu501Ter)
c.1561G>T (p.Glu521Ter)
n.1215G>T
c.1807G>T (p.Glu603Ter)
 ClinVar dbSNP
11g.64804501C=CA1978917243MEN1c.1681G= (p.Glu561=)
c.*974G= (n.*974G=)
c.1657G= (p.Glu553=)
c.1666G= (p.Glu556=)
c.*762G= (n.*762G=)
c.1008G=
n.2159G=
n.1628G=
n.2048G=
n.2167G=
n.1943G=
c.1792G= (p.Glu598=)
c.1501G= (p.Glu501=)
c.1561G= (p.Glu521=)
n.1215G=
c.1807G= (p.Glu603=)
11g.64804501C>GCA381177792MEN1c.1681G>C (p.Glu561Gln)
c.*974G>C (n.*974G>C)
c.1657G>C (p.Glu553Gln)
c.1666G>C (p.Glu556Gln)
c.*762G>C (n.*762G>C)
c.1008G>C
n.2159G>C
n.1628G>C
n.2048G>C
n.2167G>C
n.1943G>C
c.1792G>C (p.Glu598Gln)
c.1501G>C (p.Glu501Gln)
c.1561G>C (p.Glu521Gln)
n.1215G>C
c.1807G>C (p.Glu603Gln)
11g.64804501C>TCA381177794MEN1c.1681G>A (p.Glu561Lys)
c.*974G>A (n.*974G>A)
c.1657G>A (p.Glu553Lys)
c.1666G>A (p.Glu556Lys)
c.*762G>A (n.*762G>A)
c.1008G>A
n.2159G>A
n.1628G>A
n.2048G>A
n.2167G>A
n.1943G>A
c.1792G>A (p.Glu598Lys)
c.1501G>A (p.Glu501Lys)
c.1561G>A (p.Glu521Lys)
n.1215G>A
c.1807G>A (p.Glu603Lys)
11g.64804502A>CCA381177796MEN1c.1680T>G (p.Ser560Arg)
c.*973T>G (n.*973T>G)
c.1656T>G (p.Ser552Arg)
c.1665T>G (p.Ser555Arg)
c.*761T>G (n.*761T>G)
c.1007T>G
n.2158T>G
n.1627T>G
n.2047T>G
n.2166T>G
n.1942T>G
c.1791T>G (p.Ser597Arg)
c.1500T>G (p.Ser500Arg)
c.1560T>G (p.Ser520Arg)
n.1214T>G
c.1806T>G (p.Ser602Arg)
11g.64804502A>GCA475163466MEN1c.1680T>C (p.Ser560=)
c.*973T>C (n.*973T>C)
c.1656T>C (p.Ser552=)
c.1665T>C (p.Ser555=)
c.*761T>C (n.*761T>C)
c.1007T>C
n.2158T>C
n.1627T>C
n.2047T>C
n.2166T>C
n.1942T>C
c.1791T>C (p.Ser597=)
c.1500T>C (p.Ser500=)
c.1560T>C (p.Ser520=)
n.1214T>C
c.1806T>C (p.Ser602=)
11g.64804502A>TCA381177798MEN1c.1680T>A (p.Ser560Arg)
c.*973T>A (n.*973T>A)
c.1656T>A (p.Ser552Arg)
c.1665T>A (p.Ser555Arg)
c.*761T>A (n.*761T>A)
c.1007T>A
n.2158T>A
n.1627T>A
n.2047T>A
n.2166T>A
n.1942T>A
c.1791T>A (p.Ser597Arg)
c.1500T>A (p.Ser500Arg)
c.1560T>A (p.Ser520Arg)
n.1214T>A
c.1806T>A (p.Ser602Arg)

Number of alleles fetched