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
single nucleotide variant	NM_024675.4(PALB2):c.854C>G (p.Ser285Ter)	PALB2	Pathogenic	16	23647013	23647013	G	C	criteria provided, single submitter	ClinGen:CA395135849
Deletion	NM_024675.4(PALB2):c.1192del (p.Val398fs)	PALB2	Pathogenic	16	23646675	23646675	AC	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA658658427
Deletion	NM_024675.4(PALB2):c.844_847del (p.Arg282fs)	PALB2	Pathogenic	16	23647020	23647023	AATCT	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA658658438
Deletion	NM_024675.4(PALB2):c.839del (p.Asn280fs)	PALB2	Pathogenic	16	23647028	23647028	GT	G	reviewed by expert panel	ClinGen:CA494462159
Deletion	NM_024675.4(PALB2):c.1031del (p.Asn344fs)	PALB2	Pathogenic	16	23646836	23646836	GT	G	criteria provided, multiple submitters, no conflicts	ClinGen:CA621661750
Deletion	NM_024675.4(PALB2):c.901_907del (p.Asp301fs)	PALB2	Pathogenic/Likely pathogenic	16	23646960	23646966	AGGTTATC	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA658658436
single nucleotide variant	NM_024675.4(PALB2):c.682C>T (p.Gln228Ter)	PALB2	Pathogenic	16	23647185	23647185	G	A	reviewed by expert panel	ClinGen:CA395136420
Deletion	NM_024675.4(PALB2):c.639del (p.Thr214fs)	PALB2	Pathogenic	16	23647228	23647228	TA	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA658658441
Duplication	NM_024675.4(PALB2):c.3246dup (p.Glu1083Ter)	PALB2	Pathogenic	16	23619288	23619289	C	CA	criteria provided, single submitter	ClinGen:CA658658456
single nucleotide variant	NM_024675.4(PALB2):c.3130C>T (p.Gln1044Ter)	PALB2	Pathogenic/Likely pathogenic	16	23625396	23625396	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA395141418