Knowledge base for genomic medicine in Japanese
若年性ポリポーシス症候群
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_004329.3(BMPR1A):c.1081C>T (p.Arg361Ter)BMPR1APathogenic108867914188679141CTcriteria provided, multiple submitters, no conflictsClinGen:CA186249
DeletionNM_004329.3(BMPR1A):c.420del (p.Val141fs)BMPR1APathogenic108865963788659637CTCcriteria provided, single submitterClinGen:CA190154
DuplicationNM_004329.3(BMPR1A):c.216dup (p.Asn73Ter)BMPR1APathogenic108864996588649966AATcriteria provided, multiple submitters, no conflictsClinGen:CA189133
DeletionNM_004329.3(BMPR1A):c.176del (p.Phe58_Leu59insTer)BMPR1APathogenic108864992288649922CTCcriteria provided, multiple submitters, no conflictsClinGen:CA186193
single nucleotide variantNM_004329.3(BMPR1A):c.1A>G (p.Met1Val)BMPR1APathogenic/Likely pathogenic108863577688635776AGcriteria provided, multiple submitters, no conflictsClinGen:CA195612
single nucleotide variantNM_004329.3(BMPR1A):c.262G>T (p.Glu88Ter)BMPR1APathogenic108865191588651915GTcriteria provided, multiple submitters, no conflictsClinGen:CA298508
single nucleotide variantNM_004329.3(BMPR1A):c.682C>T (p.Arg228Ter)BMPR1APathogenic108867689788676897CTcriteria provided, multiple submitters, no conflictsClinGen:CA294476
single nucleotide variantNM_004329.3(BMPR1A):c.1037A>G (p.His346Arg)BMPR1ALikely pathogenic108867909788679097AGcriteria provided, single submitterClinGen:CA168682
single nucleotide variantNM_004329.3(BMPR1A):c.817C>T (p.Arg273Ter)BMPR1APathogenic108867703288677032CTcriteria provided, multiple submitters, no conflictsClinGen:CA168144
single nucleotide variantNM_004329.3(BMPR1A):c.371G>A (p.Cys124Tyr)BMPR1APathogenic/Likely pathogenic108865958888659588GAcriteria provided, multiple submitters, no conflictsClinGen:CA168082