家族性膵がん - MGenReviews

家族性膵がん

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
Deletion	NM_007294.4(BRCA1):c.5304del (p.Tyr1769fs)	BRCA1	Pathogenic	17	41203108	41203108	AG	A	reviewed by expert panel	Breast Cancer Information Core (BIC) (BRCA1):5423&base_change=del C,ClinGen:CA003457
Deletion	NM_007294.4(BRCA1):c.5311_5332+1del	BRCA1	Pathogenic	17	41203079	41203101	ACCTGTGGGCATGTTGGTGAAGGG	A	criteria provided, single submitter	Breast Cancer Information Core (BIC) (BRCA1):5430&base_change=del 23,ClinGen:CA10602574
single nucleotide variant	NM_007294.4(BRCA1):c.5332+2T>A	BRCA1	Pathogenic/Likely pathogenic	17	41203078	41203078	A	T	criteria provided, multiple submitters, no conflicts	Breast Cancer Information Core (BIC) (BRCA1):5451+2&base_change=T to A,ClinGen:CA003487
Duplication	NM_007294.4(BRCA1):c.5352dup (p.Gln1785fs)	BRCA1	Pathogenic	17	41201191	41201192	G	GT	reviewed by expert panel	Breast Cancer Information Core (BIC) (BRCA1):5471&base_change=ins A,ClinGen:CA003518
Deletion	NM_007294.4(BRCA1):c.5370_5397del (p.Val1791fs)	BRCA1	Pathogenic	17	41201147	41201174	GGGTGAATGATGAAAGCTCCTTCACCACA	G	reviewed by expert panel	Breast Cancer Information Core (BIC) (BRCA1):5489&base_change=del 28,ClinGen:CA003538
Deletion	NM_007294.4(BRCA1):c.5406+2del	BRCA1	Pathogenic	17	41201136	41201136	TA	T	criteria provided, single submitter	Breast Cancer Information Core (BIC) (BRCA1):5525+2&base_change=del T,ClinGen:CA268394
single nucleotide variant	NM_007294.4(BRCA1):c.5407-1G>A	BRCA1	Pathogenic	17	41199721	41199721	C	T	criteria provided, multiple submitters, no conflicts	Breast Cancer Information Core (BIC) (BRCA1):5526-1&base_change=G to A,ClinGen:CA003569
single nucleotide variant	NM_007294.4(BRCA1):c.5407-1G>C	BRCA1	Pathogenic/Likely pathogenic	17	41199721	41199721	C	G	criteria provided, multiple submitters, no conflicts	Breast Cancer Information Core (BIC) (BRCA1):5526-1&base_change=G to C,ClinGen:CA003570
Insertion	NM_007294.4(BRCA1):c.5464_5465insT (p.His1822fs)	BRCA1	Pathogenic	17	41199662	41199663	T	TA	reviewed by expert panel	ClinGen:CA003609
single nucleotide variant	NM_007294.4(BRCA1):c.5467+2T>C	BRCA1	Pathogenic/Likely pathogenic	17	41199658	41199658	A	G	criteria provided, multiple submitters, no conflicts	Breast Cancer Information Core (BIC) (BRCA1):5586+2&base_change=T to C,ClinGen:CA003611