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.675+1G>CBMPR1ALikely pathogenic108867214288672142GCcriteria provided, single submitterClinGen:CA10582746
DeletionNM_004329.2(BMPR1A):c.-152-?_*1469delBMPR1APathogenic108863562488684945nanacriteria provided, single submitter-
IndelNM_004329.3(BMPR1A):c.884delinsGTTCATAGCGG (p.Asp295delinsGlySerTer)BMPR1APathogenic108867894488678944AGTTCATAGCGGcriteria provided, single submitterClinGen:CA10578889
DuplicationNM_004329.3(BMPR1A):c.405dup (p.Pro136fs)BMPR1APathogenic108865962088659621CCAcriteria provided, multiple submitters, no conflictsClinGen:CA10578878
single nucleotide variantNM_004329.3(BMPR1A):c.309T>G (p.Tyr103Ter)BMPR1APathogenic108865196288651962TGcriteria provided, single submitterClinGen:CA10578876
single nucleotide variantNM_004329.3(BMPR1A):c.246C>A (p.Cys82Ter)BMPR1APathogenic108865189988651899CAcriteria provided, single submitterClinGen:CA10578874
DuplicationNM_004329.3(BMPR1A):c.286_289dup (p.Ala97fs)BMPR1APathogenic108865193888651939AATTAGcriteria provided, single submitterClinGen:CA353504
single nucleotide variantNM_004329.3(BMPR1A):c.3G>C (p.Met1Ile)BMPR1APathogenic/Likely pathogenic108863577888635778GCcriteria provided, multiple submitters, no conflictsClinGen:CA353511
DeletionNM_004329.3(BMPR1A):c.247_251del (p.Phe83fs)BMPR1APathogenic108865189688651900ATTGCTAcriteria provided, multiple submitters, no conflictsClinGen:CA334485
single nucleotide variantNM_004329.3(BMPR1A):c.1480C>T (p.Arg494Ter)BMPR1APathogenic/Likely pathogenic108868335788683357CTcriteria provided, multiple submitters, no conflictsClinGen:CA186232