多発性内分泌腫瘍症1型、2A・2B型／甲状腺髄様がん

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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
single nucleotide variant	NM_020975.6(RET):c.1825T>C (p.Cys609Arg)	RET	Pathogenic	10	43609069	43609069	T	C	criteria provided, multiple submitters, no conflicts	ClinGen:CA007804,UniProtKB:P07949#VAR_009471,OMIM:164761.0042
single nucleotide variant	NM_020975.6(RET):c.1826G>A (p.Cys609Tyr)	RET	Pathogenic	10	43609070	43609070	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA007824,UniProtKB:P07949#VAR_006306,OMIM:164761.0029
single nucleotide variant	NM_020975.6(RET):c.1826G>T (p.Cys609Phe)	RET	Pathogenic	10	43609070	43609070	G	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA007843
single nucleotide variant	NM_020975.6(RET):c.1826G>C (p.Cys609Ser)	RET	Pathogenic	10	43609070	43609070	G	C	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_020975.6(RET):c.1827C>G (p.Cys609Trp)	RET	Pathogenic	10	43609071	43609071	C	G	criteria provided, single submitter	UniProtKB:P07949#VAR_006307
single nucleotide variant	NM_020975.6(RET):c.1831T>C (p.Cys611Arg)	RET	Likely pathogenic	10	43609075	43609075	T	C	criteria provided, single submitter	ClinGen:CA007873,UniProtKB:P07949#VAR_009473
single nucleotide variant	NM_020975.6(RET):c.1831T>G (p.Cys611Gly)	RET	Pathogenic	10	43609075	43609075	T	G	criteria provided, multiple submitters, no conflicts	ClinGen:CA007883,UniProtKB:P07949#VAR_009472
single nucleotide variant	NM_020975.6(RET):c.1831T>A (p.Cys611Ser)	RET	Pathogenic	10	43609075	43609075	T	A	criteria provided, single submitter	UniProtKB:P07949#VAR_009474
single nucleotide variant	NM_020975.6(RET):c.1832G>A (p.Cys611Tyr)	RET	Pathogenic	10	43609076	43609076	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA007934,UniProtKB:P07949#VAR_006309
single nucleotide variant	NM_020975.6(RET):c.1832G>T (p.Cys611Phe)	RET	Pathogenic	10	43609076	43609076	G	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA007949