若年性ポリポーシス症候群

腫瘍性疾患

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Type	Name	Gene Symbol	Clinical Significance	Chromosome	Start	Stop	Reference Allele	Alternate Allele	Review Status	Other IDs
Type	Name	Gene Symbol	Clinical Significance	Chromosome	(GRCh37)		Reference Allele	Alternate Allele	Review Status	Other IDs
single nucleotide variant	NM_004329.3(BMPR1A):c.1A>C (p.Met1Leu)	BMPR1A	Pathogenic/Likely pathogenic	10	88635776	88635776	A	C	criteria provided, multiple submitters, no conflicts	ClinGen:CA377774739
single nucleotide variant	NM_004329.3(BMPR1A):c.67G>A (p.Gly23Arg)	BMPR1A	Likely pathogenic	10	88635842	88635842	G	A	criteria provided, single submitter	ClinGen:CA377774875
single nucleotide variant	NM_004329.3(BMPR1A):c.68-1G>C	BMPR1A	Pathogenic	10	88649818	88649818	G	C	criteria provided, single submitter	ClinGen:CA377446197
Deletion	NM_004329.3(BMPR1A):c.160del (p.Asp54fs)	BMPR1A	Pathogenic	10	88649910	88649910	AG	A	criteria provided, single submitter	ClinGen:CA645369466
Deletion	NM_004329.3(BMPR1A):c.367del (p.Glu123fs)	BMPR1A	Pathogenic	10	88659584	88659584	AG	A	criteria provided, single submitter	ClinGen:CA645369423
single nucleotide variant	NM_004329.3(BMPR1A):c.373T>G (p.Cys125Gly)	BMPR1A	Pathogenic	10	88659590	88659590	T	G	criteria provided, single submitter	ClinGen:CA377449439
single nucleotide variant	NM_004329.3(BMPR1A):c.388T>C (p.Cys130Arg)	BMPR1A	Pathogenic	10	88659605	88659605	T	C	criteria provided, single submitter	ClinGen:CA377449596
Indel	NM_004329.3(BMPR1A):c.441_458delinsGA (p.Phe147fs)	BMPR1A	Pathogenic	10	88659794	88659811	TGATGGCAGCATTCGATG	GA	criteria provided, multiple submitters, no conflicts	ClinGen:CA645369424
single nucleotide variant	NM_004329.3(BMPR1A):c.454C>T (p.Arg152Ter)	BMPR1A	Pathogenic	10	88659807	88659807	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA377450232
single nucleotide variant	NM_004329.3(BMPR1A):c.458G>A (p.Trp153Ter)	BMPR1A	Pathogenic	10	88659811	88659811	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA377450259