Knowledge base for genomic medicine in Japanese
遺伝性混合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.964A>T (p.Lys322Ter)BMPR1APathogenic108867902488679024ATcriteria provided, single submitterClinGen:CA377460285
DuplicationNM_004329.3(BMPR1A):c.1058_1059dup (p.Gly354fs)BMPR1APathogenic108867911788679118CCAAcriteria provided, single submitterClinGen:CA645369465
single nucleotide variantNM_004329.3(BMPR1A):c.1221C>G (p.Tyr407Ter)BMPR1APathogenic/Likely pathogenic108868133188681331CGcriteria provided, multiple submitters, no conflictsClinGen:CA377461997
single nucleotide variantNM_004329.3(BMPR1A):c.1460G>A (p.Trp487Ter)BMPR1APathogenic108868325088683250GAcriteria provided, single submitterClinGen:CA377463185
single nucleotide variantNM_004329.3(BMPR1A):c.64C>T (p.Gln22Ter)BMPR1APathogenic108863583988635839CTcriteria provided, multiple submitters, no conflictsClinGen:CA377774871
single nucleotide variantNM_004329.3(BMPR1A):c.697C>T (p.Gln233Ter)BMPR1APathogenic/Likely pathogenic108867691288676912CTcriteria provided, multiple submitters, no conflictsClinGen:CA377457014
DuplicationNM_004329.3(BMPR1A):c.578dup (p.Leu193fs)BMPR1APathogenic108867204188672042AATcriteria provided, single submitterClinGen:CA658657981
single nucleotide variantNM_004329.3(BMPR1A):c.834C>A (p.Tyr278Ter)BMPR1APathogenic108867704988677049CAcriteria provided, single submitterClinGen:CA377458622
single nucleotide variantNM_004329.3(BMPR1A):c.567C>A (p.Tyr189Ter)BMPR1APathogenic108867203388672033CAcriteria provided, single submitterClinGen:CA377454413
DuplicationNM_004329.3(BMPR1A):c.957dup (p.Phe320fs)BMPR1APathogenic108867901688679017AACcriteria provided, single submitterClinGen:CA658657987