遺伝性乳がん・卵巣がん症候群

腫瘍性疾患

表のタイトル行が青色の項目は、クリックすることでソートすることができます。

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_000059.4(BRCA2):c.1992del (p.Thr665fs)	BRCA2	Pathogenic	13	32910482	32910482	TG	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA658656350
Deletion	NM_000059.4(BRCA2):c.2272del (p.Ser758fs)	BRCA2	Pathogenic	13	32910761	32910761	GA	G	criteria provided, multiple submitters, no conflicts	ClinGen:CA658656370
Indel	NM_000059.4(BRCA2):c.7833_7843delinsG (p.Asp2611fs)	BRCA2	Pathogenic	13	32936687	32936697	TCCAAAGCTTA	G	criteria provided, single submitter	ClinGen:CA658656477
Duplication	NM_000059.4(BRCA2):c.9330dup (p.Glu3111Ter)	BRCA2	Pathogenic	13	32968898	32968899	A	AT	criteria provided, single submitter	ClinGen:CA658656359
single nucleotide variant	NM_000059.4(BRCA2):c.9919A>T (p.Lys3307Ter)	BRCA2	Pathogenic	13	32972569	32972569	A	T	criteria provided, single submitter	ClinGen:CA387767049
Duplication	NM_000059.4(BRCA2):c.3620_3621dup (p.Leu1208fs)	BRCA2	Pathogenic	13	32912110	32912111	T	TTA	criteria provided, single submitter	ClinGen:CA658656419
Deletion	NM_000059.4(BRCA2):c.4013_4014del (p.Gly1338fs)	BRCA2	Pathogenic	13	32912505	32912506	GGC	G	criteria provided, single submitter	ClinGen:CA658656332
single nucleotide variant	NM_000059.4(BRCA2):c.4411A>T (p.Arg1471Ter)	BRCA2	Pathogenic	13	32912903	32912903	A	T	criteria provided, single submitter	ClinGen:CA387781188
Deletion	NM_000059.4(BRCA2):c.4884_4885del (p.Lys1628fs)	BRCA2	Pathogenic	13	32913374	32913375	CAA	C	criteria provided, multiple submitters, no conflicts	ClinGen:CA658656364
Duplication	NM_000059.4(BRCA2):c.5205dup (p.Gln1736fs)	BRCA2	Pathogenic	13	32913692	32913693	G	GA	criteria provided, single submitter	ClinGen:CA658656382