MUTYH関連ポリポーシス

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_001048174.2(MUTYH):c.1017del (p.Arg340fs)	MUTYH	Pathogenic	1	45797418	45797418	TG	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA522810414
single nucleotide variant	NM_001048174.2(MUTYH):c.1102+1G>T	MUTYH	Pathogenic/Likely pathogenic	1	45797332	45797332	C	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA340133234
single nucleotide variant	NM_001048174.2(MUTYH):c.268G>T (p.Glu90Ter)	MUTYH	Pathogenic/Likely pathogenic	1	45798993	45798993	C	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA340136310
single nucleotide variant	NM_001128425.2(MUTYH):c.36+1G>A	MUTYH	Likely pathogenic	1	45805890	45805890	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA340137825
single nucleotide variant	NM_001128425.2(MUTYH):c.36G>A (p.Trp12Ter)	MUTYH	Pathogenic	1	45805891	45805891	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA340137829
single nucleotide variant	NM_001048174.2(MUTYH):c.224G>A (p.Trp75Ter)	MUTYH	Pathogenic	1	45799125	45799125	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA340136412
single nucleotide variant	NM_001048174.2(MUTYH):c.264+1G>T	MUTYH	Likely pathogenic	1	45799084	45799084	C	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA340136330
single nucleotide variant	NM_001048174.2(MUTYH):c.606G>A (p.Gln202=)	MUTYH	Pathogenic/Likely pathogenic	1	45798246	45798246	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA21838430
single nucleotide variant	NM_001048174.2(MUTYH):c.164C>G (p.Ser55Ter)	MUTYH	Pathogenic/Likely pathogenic	1	45799185	45799185	G	C	criteria provided, multiple submitters, no conflicts	ClinGen:CA057154
Deletion	NM_001048174.2(MUTYH):c.492+1del	MUTYH	Likely pathogenic	1	45798434	45798434	AC	A	criteria provided, single submitter	ClinGen:CA658656928