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.64804488C>ACA381177721MEN1c.1694G>T (p.Gly565Val)
c.*987G>T (n.*987G>T)
c.1670G>T (p.Gly557Val)
c.1679G>T (p.Gly560Val)
c.*775G>T (n.*775G>T)
c.1021G>T
n.2172G>T
n.1641G>T
n.2180G>T
n.1956G>T
c.1805G>T (p.Gly602Val)
c.1514G>T (p.Gly505Val)
c.1574G>T (p.Gly525Val)
n.1228G>T
c.1820G>T (p.Gly607Val)
dbSNP
11g.64804488C>GCA381177723MEN1c.1694G>C (p.Gly565Ala)
c.*987G>C (n.*987G>C)
c.1670G>C (p.Gly557Ala)
c.1679G>C (p.Gly560Ala)
c.*775G>C (n.*775G>C)
c.1021G>C
n.2172G>C
n.1641G>C
n.2180G>C
n.1956G>C
c.1805G>C (p.Gly602Ala)
c.1514G>C (p.Gly505Ala)
c.1574G>C (p.Gly525Ala)
n.1228G>C
c.1820G>C (p.Gly607Ala)
11g.64804488C>TCA381177724MEN1c.1694G>A (p.Gly565Asp)
c.*987G>A (n.*987G>A)
c.1670G>A (p.Gly557Asp)
c.1679G>A (p.Gly560Asp)
c.*775G>A (n.*775G>A)
c.1021G>A
n.2172G>A
n.1641G>A
n.2180G>A
n.1956G>A
c.1805G>A (p.Gly602Asp)
c.1514G>A (p.Gly505Asp)
c.1574G>A (p.Gly525Asp)
n.1228G>A
c.1820G>A (p.Gly607Asp)
11g.64804490delCA2695214495MEN1c.1694del (p.Gly565AlafsTer2)
c.*987del (n.*987del)
c.1670del (p.Gly557AlafsTer2)
c.1679del (p.Gly560AlafsTer2)
c.*775del (n.*775del)
c.1021del
n.2172del
n.1641del
n.2180del
n.1956del
c.1805del (p.Gly602AlafsTer2)
c.1514del (p.Gly505AlafsTer2)
c.1574del (p.Gly525AlafsTer2)
n.1228del
c.1820del (p.Gly607AlafsTer2)
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.64804489C>ACA381177725MEN1c.1693G>T (p.Gly565Cys)
c.*986G>T (n.*986G>T)
c.1669G>T (p.Gly557Cys)
c.1678G>T (p.Gly560Cys)
c.*774G>T (n.*774G>T)
c.1020G>T
n.2171G>T
n.1640G>T
n.2179G>T
n.1955G>T
c.1804G>T (p.Gly602Cys)
c.1513G>T (p.Gly505Cys)
c.1573G>T (p.Gly525Cys)
n.1227G>T
c.1819G>T (p.Gly607Cys)
11g.64804489C>GCA381177727MEN1c.1693G>C (p.Gly565Arg)
c.*986G>C (n.*986G>C)
c.1669G>C (p.Gly557Arg)
c.1678G>C (p.Gly560Arg)
c.*774G>C (n.*774G>C)
c.1020G>C
n.2171G>C
n.1640G>C
n.2179G>C
n.1955G>C
c.1804G>C (p.Gly602Arg)
c.1513G>C (p.Gly505Arg)
c.1573G>C (p.Gly525Arg)
n.1227G>C
c.1819G>C (p.Gly607Arg)
11g.64804489C>TCA381177728MEN1c.1693G>A (p.Gly565Ser)
c.*986G>A (n.*986G>A)
c.1669G>A (p.Gly557Ser)
c.1678G>A (p.Gly560Ser)
c.*774G>A (n.*774G>A)
c.1020G>A
n.2171G>A
n.1640G>A
n.2179G>A
n.1955G>A
c.1804G>A (p.Gly602Ser)
c.1513G>A (p.Gly505Ser)
c.1573G>A (p.Gly525Ser)
n.1227G>A
c.1819G>A (p.Gly607Ser)
ClinVar dbSNP
11g.64804490C>ACA381177730MEN1c.1692G>T (p.Lys564Asn)
c.*985G>T (n.*985G>T)
c.1668G>T (p.Lys556Asn)
c.1677G>T (p.Lys559Asn)
c.*773G>T (n.*773G>T)
c.1019G>T
n.2170G>T
n.1639G>T
n.2059G>T
n.2178G>T
n.1954G>T
c.1803G>T (p.Lys601Asn)
c.1512G>T (p.Lys504Asn)
c.1572G>T (p.Lys524Asn)
n.1226G>T
c.1818G>T (p.Lys606Asn)
dbSNP
11g.64804490C>GCA381177732MEN1c.1692G>C (p.Lys564Asn)
c.*985G>C (n.*985G>C)
c.1668G>C (p.Lys556Asn)
c.1677G>C (p.Lys559Asn)
c.*773G>C (n.*773G>C)
c.1019G>C
n.2170G>C
n.1639G>C
n.2059G>C
n.2178G>C
n.1954G>C
c.1803G>C (p.Lys601Asn)
c.1512G>C (p.Lys504Asn)
c.1572G>C (p.Lys524Asn)
n.1226G>C
c.1818G>C (p.Lys606Asn)
11g.64804490C>TCA475163403MEN1c.1692G>A (p.Lys564=)
c.*985G>A (n.*985G>A)
c.1668G>A (p.Lys556=)
c.1677G>A (p.Lys559=)
c.*773G>A (n.*773G>A)
c.1019G>A
n.2170G>A
n.1639G>A
n.2059G>A
n.2178G>A
n.1954G>A
c.1803G>A (p.Lys601=)
c.1512G>A (p.Lys504=)
c.1572G>A (p.Lys524=)
n.1226G>A
c.1818G>A (p.Lys606=)
ClinVar dbSNP gnomAD v4
11g.64804491T>ACA381177738MEN1c.1691A>T (p.Lys564Met)
c.*984A>T (n.*984A>T)
c.1667A>T (p.Lys556Met)
c.1676A>T (p.Lys559Met)
c.*772A>T (n.*772A>T)
c.1018A>T
n.2169A>T
n.1638A>T
n.2058A>T
n.2177A>T
n.1953A>T
c.1802A>T (p.Lys601Met)
c.1511A>T (p.Lys504Met)
c.1571A>T (p.Lys524Met)
n.1225A>T
c.1817A>T (p.Lys606Met)
11g.64804491T>CCA381177736MEN1c.1691A>G (p.Lys564Arg)
c.*984A>G (n.*984A>G)
c.1667A>G (p.Lys556Arg)
c.1676A>G (p.Lys559Arg)
c.*772A>G (n.*772A>G)
c.1018A>G
n.2169A>G
n.1638A>G
n.2058A>G
n.2177A>G
n.1953A>G
c.1802A>G (p.Lys601Arg)
c.1511A>G (p.Lys504Arg)
c.1571A>G (p.Lys524Arg)
n.1225A>G
c.1817A>G (p.Lys606Arg)
gnomAD v4
11g.64804491T>GCA381177734MEN1c.1691A>C (p.Lys564Thr)
c.*984A>C (n.*984A>C)
c.1667A>C (p.Lys556Thr)
c.1676A>C (p.Lys559Thr)
c.*772A>C (n.*772A>C)
c.1018A>C
n.2169A>C
n.1638A>C
n.2058A>C
n.2177A>C
n.1953A>C
c.1802A>C (p.Lys601Thr)
c.1511A>C (p.Lys504Thr)
c.1571A>C (p.Lys524Thr)
n.1225A>C
c.1817A>C (p.Lys606Thr)
11g.64804492delCA2695214496MEN1c.1691del (p.Lys564ArgfsTer3)
c.*984del (n.*984del)
c.1667del (p.Lys556ArgfsTer3)
c.1676del (p.Lys559ArgfsTer3)
c.*772del (n.*772del)
c.1018del
n.2169del
n.1638del
n.2058del
n.2177del
n.1953del
c.1802del (p.Lys601ArgfsTer3)
c.1511del (p.Lys504ArgfsTer3)
c.1571del (p.Lys524ArgfsTer3)
n.1225del
c.1817del (p.Lys606ArgfsTer3)
11g.64804492T>ACA381177740MEN1c.1690A>T (p.Lys564Ter)
c.*983A>T (n.*983A>T)
c.1666A>T (p.Lys556Ter)
c.1675A>T (p.Lys559Ter)
c.*771A>T (n.*771A>T)
c.1017A>T
n.2168A>T
n.1637A>T
n.2057A>T
n.2176A>T
n.1952A>T
c.1801A>T (p.Lys601Ter)
c.1510A>T (p.Lys504Ter)
c.1570A>T (p.Lys524Ter)
n.1224A>T
c.1816A>T (p.Lys606Ter)
ClinVar
11g.64804492T>CCA381177743MEN1c.1690A>G (p.Lys564Glu)
c.*983A>G (n.*983A>G)
c.1666A>G (p.Lys556Glu)
c.1675A>G (p.Lys559Glu)
c.*771A>G (n.*771A>G)
c.1017A>G
n.2168A>G
n.1637A>G
n.2057A>G
n.2176A>G
n.1952A>G
c.1801A>G (p.Lys601Glu)
c.1510A>G (p.Lys504Glu)
c.1570A>G (p.Lys524Glu)
n.1224A>G
c.1816A>G (p.Lys606Glu)
11g.64804492T>GCA381177742MEN1c.1690A>C (p.Lys564Gln)
c.*983A>C (n.*983A>C)
c.1666A>C (p.Lys556Gln)
c.1675A>C (p.Lys559Gln)
c.*771A>C (n.*771A>C)
c.1017A>C
n.2168A>C
n.1637A>C
n.2057A>C
n.2176A>C
n.1952A>C
c.1801A>C (p.Lys601Gln)
c.1510A>C (p.Lys504Gln)
c.1570A>C (p.Lys524Gln)
n.1224A>C
c.1816A>C (p.Lys606Gln)
11g.64804492T=CA1978917187MEN1c.1690A= (p.Lys564=)
c.*983A= (n.*983A=)
c.1666A= (p.Lys556=)
c.1675A= (p.Lys559=)
c.*771A= (n.*771A=)
c.1017A=
n.2168A=
n.1637A=
n.2057A=
n.2176A=
n.1952A=
c.1801A= (p.Lys601=)
c.1510A= (p.Lys504=)
c.1570A= (p.Lys524=)
n.1224A=
c.1816A= (p.Lys606=)
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)
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)
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

Number of alleles fetched