Knowledge base for genomic medicine in Japanese
多発性内分泌腫瘍症1型、2A・2B型/甲状腺髄様がん
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_001370259.2(MEN1):c.340dup (p.Ser114fs)MEN1Pathogenic116457724164577242CCTcriteria provided, multiple submitters, no conflictsClinGen:CA10603131
DuplicationNM_020975.6(RET):c.890dup (p.Val298fs)RETPathogenic104360184543601846CCGcriteria provided, single submitterClinGen:CA10603140
DuplicationNM_001370259.2(MEN1):c.1429dup (p.Glu477fs)MEN1Pathogenic116457220964572210TTCcriteria provided, single submitterClinGen:CA10603166
IndelNM_001370259.2(MEN1):c.490_491delinsT (p.Ala164fs)MEN1Pathogenic116457552664575527GCAcriteria provided, single submitterClinGen:CA10603168
single nucleotide variantNM_001370259.2(MEN1):c.446-2A>CMEN1Pathogenic116457557364575573TGcriteria provided, multiple submitters, no conflictsClinGen:CA10603221
single nucleotide variantNM_020975.6(RET):c.2418C>G (p.Tyr806Ter)RETPathogenic104361500443615004CGcriteria provided, single submitterClinGen:CA10606962
DuplicationNM_001370259.2(MEN1):c.773_775dup (p.Gln258dup)MEN1Likely pathogenic116457503164575032AAGCTcriteria provided, single submitterClinGen:CA16042754
DeletionNM_001370259.2(MEN1):c.207del (p.Asp70fs)MEN1Pathogenic116457737564577375CGCcriteria provided, single submitterClinGen:CA16042759
single nucleotide variantNM_001370259.2(MEN1):c.913-1G>AMEN1Pathogenic/Likely pathogenic116457384164573841CTcriteria provided, multiple submitters, no conflictsClinGen:CA16042860
DeletionNM_001370259.2(MEN1):c.654+1delMEN1Pathogenic116457536264575362ACAcriteria provided, single submitterClinGen:CA16043460