家族性副甲状腺機能亢進症 (MEN以外)

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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_000388.4(CASR):c.1884del (p.Phe629fs)	CASR	Likely pathogenic	3	122002684	122002684	GC	G	criteria provided, single submitter	ClinGen:CA213574
single nucleotide variant	NM_000388.4(CASR):c.1934C>A (p.Ala645Asp)	CASR	Likely pathogenic	3	122002735	122002735	C	A	criteria provided, single submitter	ClinGen:CA213575
single nucleotide variant	NM_000388.4(CASR):c.2014C>A (p.Pro672Thr)	CASR	Likely pathogenic	3	122002815	122002815	C	A	criteria provided, single submitter	ClinGen:CA213577
single nucleotide variant	NM_000388.4(CASR):c.2243C>A (p.Pro748Gln)	CASR	Likely pathogenic	3	122003044	122003044	C	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA213582
single nucleotide variant	NM_000388.4(CASR):c.2435T>C (p.Leu812Pro)	CASR	Likely pathogenic	3	122003236	122003236	T	C	criteria provided, single submitter	ClinGen:CA213586
single nucleotide variant	NM_000388.4(CASR):c.2644A>T (p.Lys882Ter)	CASR	Likely pathogenic	3	122003445	122003445	A	T	criteria provided, single submitter	ClinGen:CA213590
single nucleotide variant	NM_000388.4(CASR):c.380A>G (p.Glu127Gly)	CASR	Likely pathogenic	3	121976122	121976122	A	G	criteria provided, multiple submitters, no conflicts	ClinGen:CA213599
single nucleotide variant	NM_000388.4(CASR):c.643G>C (p.Asp215His)	CASR	Likely pathogenic	3	121980525	121980525	G	C	criteria provided, single submitter	ClinGen:CA213604
single nucleotide variant	NM_000388.4(CASR):c.974G>A (p.Gly325Glu)	CASR	Likely pathogenic	3	121980856	121980856	G	A	criteria provided, single submitter	ClinGen:CA213606
single nucleotide variant	NM_000388.4(CASR):c.2482A>C (p.Thr828Pro)	CASR	Likely pathogenic	3	122003283	122003283	A	C	criteria provided, single submitter	ClinGen:CA203861