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_024675.4(PALB2):c.2100_2110del (p.Ser701fs)	PALB2	Pathogenic	16	23641365	23641375	AGTAATATGGAT	A	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_024675.4(PALB2):c.1845del (p.Asp616fs)	PALB2	Likely pathogenic	16	23641630	23641630	CA	C	criteria provided, single submitter	-
Deletion	NM_024675.4(PALB2):c.1789del (p.Met597fs)	PALB2	Pathogenic	16	23641686	23641686	AT	A	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_024675.4(PALB2):c.1288C>T (p.Gln430Ter)	PALB2	Pathogenic/Likely pathogenic	16	23646579	23646579	G	A	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_024675.4(PALB2):c.1227_1231del (p.Tyr409_Arg411delinsTer)	PALB2	Pathogenic/Likely pathogenic	16	23646636	23646640	CTAACA	C	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_024675.4(PALB2):c.841del (p.Ile281fs)	PALB2	Likely pathogenic	16	23647026	23647026	AT	A	criteria provided, single submitter	-
Duplication	NM_024675.4(PALB2):c.820dup (p.Thr274fs)	PALB2	Pathogenic/Likely pathogenic	16	23647046	23647047	G	GT	criteria provided, multiple submitters, no conflicts	-
Insertion	NM_024675.4(PALB2):c.774_775insC (p.Ser259fs)	PALB2	Likely pathogenic	16	23647092	23647093	T	TG	criteria provided, single submitter	-
Deletion	NM_024675.4(PALB2):c.770del (p.Gly257fs)	PALB2	Likely pathogenic	16	23647097	23647097	AC	A	criteria provided, single submitter	-
Duplication	NM_024675.4(PALB2):c.502dup (p.Ser168fs)	PALB2	Pathogenic	16	23647364	23647365	G	GA	criteria provided, multiple submitters, no conflicts	-