アルカプトン尿症

小児・神経疾患

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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
Indel	NM_000187.4(HGD):c.1017_1019delinsTA (p.Met339fs)	HGD	Pathogenic	3	120352163	120352165	CTC	TA	criteria provided, multiple submitters, no conflicts	ClinGen:CA16040886
Duplication	NM_000187.4(HGD):c.970dup (p.Val324fs)	HGD	Pathogenic/Likely pathogenic	3	120357337	120357338	A	AC	criteria provided, multiple submitters, no conflicts	ClinGen:CA16040887
Deletion	NM_000187.4(HGD):c.956del (p.Pro319fs)	HGD	Likely pathogenic	3	120357352	120357352	TG	T	criteria provided, single submitter	ClinGen:CA16040888
Duplication	NM_000187.4(HGD):c.781dup (p.Ser261fs)	HGD	Likely pathogenic	3	120360533	120360534	G	GA	criteria provided, single submitter	ClinGen:CA16040889
single nucleotide variant	NM_000187.4(HGD):c.649+2T>C	HGD	Likely pathogenic	3	120365112	120365112	A	G	criteria provided, single submitter	ClinGen:CA16040890
Deletion	NM_000187.4(HGD):c.409del (p.Leu137fs)	HGD	Likely pathogenic	3	120369646	120369646	AG	A	criteria provided, single submitter	ClinGen:CA16040891
Deletion	NM_000187.4(HGD):c.390del (p.Ala132fs)	HGD	Likely pathogenic	3	120369665	120369665	GC	G	criteria provided, single submitter	ClinGen:CA16040892
Deletion	NM_000187.4(HGD):c.376_377del (p.Lys126fs)	HGD	Likely pathogenic	3	120369678	120369679	CTT	C	criteria provided, single submitter	ClinGen:CA16040893
Deletion	NM_000187.4(HGD):c.346del (p.Leu116fs)	HGD	Likely pathogenic	3	120369709	120369709	AG	A	criteria provided, single submitter	ClinGen:CA16040894
Deletion	NM_000187.4(HGD):c.339_342+2del	HGD	Likely pathogenic	3	120371437	120371442	TACACTC	T	criteria provided, single submitter	ClinGen:CA16040895