家族性膵がん - MGenReviews

家族性膵がん

腫瘍性疾患

疾患の紹介

病的バリアントリスト

Excelでダウンロード

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最新の情報は下記 URL でご確認いただけます (外部サイトへ移動します) 。

https://ftp.ncbi.nlm.nih.gov/pub/clinvar/tab_delimited/archive/

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.3773_3774del (p.Ile1258fs)	BRCA2	Pathogenic	13	32912264	32912265	AAT	A	reviewed by expert panel	ClinGen:CA018782
Deletion	NM_000059.4(BRCA2):c.3778_3779del (p.Leu1260fs)	BRCA2	Pathogenic	13	32912269	32912270	GTT	G	reviewed by expert panel	ClinGen:CA018795
single nucleotide variant	NM_000059.4(BRCA2):c.3785C>G (p.Ser1262Ter)	BRCA2	Pathogenic	13	32912277	32912277	C	G	reviewed by expert panel	ClinGen:CA018810
single nucleotide variant	NM_000059.4(BRCA2):c.37G>T (p.Glu13Ter)	BRCA2	Pathogenic	13	32890634	32890634	G	T	reviewed by expert panel	ClinGen:CA018834
Deletion	NM_000059.4(BRCA2):c.37_44del (p.Phe12_Glu13insTer)	BRCA2	Pathogenic	13	32890630	32890637	TTTTTGAAA	T	reviewed by expert panel	ClinGen:CA018705
single nucleotide variant	NM_000059.4(BRCA2):c.3812C>A (p.Ser1271Ter)	BRCA2	Pathogenic	13	32912304	32912304	C	A	reviewed by expert panel	ClinGen:CA018857
Deletion	NM_000059.4(BRCA2):c.3824_3827del (p.Ile1275fs)	BRCA2	Pathogenic	13	32912313	32912316	AAGAT	A	reviewed by expert panel	ClinGen:CA018874
Deletion	NM_000059.4(BRCA2):c.3830del (p.Asn1277fs)	BRCA2	Pathogenic	13	32912319	32912319	GA	G	reviewed by expert panel	ClinGen:CA018884
Deletion	NM_000059.4(BRCA2):c.3836del (p.Asn1279fs)	BRCA2	Pathogenic	13	32912327	32912327	TA	T	reviewed by expert panel	ClinGen:CA018897
Deletion	NM_000059.4(BRCA2):c.3837del (p.Asn1279fs)	BRCA2	Pathogenic	13	32912329	32912329	AT	A	reviewed by expert panel	Breast Cancer Information Core (BIC) (BRCA2):4065&base_change=del T,ClinGen:CA018900

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