遺伝性乳がん (ATM/CHEK2)

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
Indel	NM_000051.4(ATM):c.8565_8566delinsAA (p.Ser2855_Val2856delinsArgIle)	ATM	Pathogenic/Likely pathogenic	11	108216616	108216617	TG	AA	criteria provided, multiple submitters, no conflicts	ClinGen:CA293967
single nucleotide variant	NM_000051.4(ATM):c.8473C>T (p.Gln2825Ter)	ATM	Pathogenic	11	108216524	108216524	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA163889
Deletion	NM_000051.4(ATM):c.378del (p.Asp126fs)	ATM	Pathogenic/Likely pathogenic	11	108106443	108106443	AT	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA164294
single nucleotide variant	NM_000051.4(ATM):c.967A>G (p.Ile323Val)	ATM	Pathogenic/Likely pathogenic	11	108117756	108117756	A	G	criteria provided, multiple submitters, no conflicts	ClinGen:CA164527,UniProtKB:Q13315#VAR_010803
single nucleotide variant	NM_000051.4(ATM):c.283C>T (p.Gln95Ter)	ATM	Pathogenic/Likely pathogenic	11	108100002	108100002	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA164660
single nucleotide variant	NM_000051.4(ATM):c.2921+1G>A	ATM	Pathogenic/Likely pathogenic	11	108141874	108141874	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA164701
single nucleotide variant	NM_000051.4(ATM):c.6095+1G>A	ATM	Likely pathogenic	11	108186639	108186639	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA164796
single nucleotide variant	NM_007194.4(CHEK2):c.151C>T (p.Gln51Ter)	CHEK2	Pathogenic/Likely pathogenic	22	29130559	29130559	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA164865
single nucleotide variant	NM_000051.4(ATM):c.7913G>A (p.Trp2638Ter)	ATM	Pathogenic/Likely pathogenic	11	108203613	108203613	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA294097
single nucleotide variant	NM_000051.4(ATM):c.8505C>A (p.Cys2835Ter)	ATM	Pathogenic/Likely pathogenic	11	108216556	108216556	C	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA164890