海綿状血管腫 - MGenReviews

海綿状血管腫

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
single nucleotide variant	NM_194454.3(KRIT1):c.845+1G>A	KRIT1	Pathogenic	7	91864121	91864121	C	T	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_194454.3(KRIT1):c.842del (p.Asp281fs)	KRIT1	Pathogenic	7	91864125	91864125	GT	G	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_194454.3(KRIT1):c.790_794del (p.Gln264fs)	KRIT1	Likely pathogenic	7	91864173	91864177	TATTTG	T	criteria provided, single submitter	-
single nucleotide variant	NM_194454.3(KRIT1):c.730-1G>A	KRIT1	Pathogenic	7	91864238	91864238	C	T	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_194454.3(KRIT1):c.729+1G>A	KRIT1	Pathogenic/Likely pathogenic	7	91864716	91864716	C	T	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_194454.3(KRIT1):c.707C>G (p.Ser236Ter)	KRIT1	Likely pathogenic	7	91864739	91864739	G	C	criteria provided, single submitter	-
Duplication	NM_194454.3(KRIT1):c.679dup (p.Thr227fs)	KRIT1	Pathogenic	7	91864766	91864767	G	GT	criteria provided, single submitter	-
Deletion	NM_194454.3(KRIT1):c.674del (p.Ala225fs)	KRIT1	Pathogenic/Likely pathogenic	7	91864772	91864772	TG	T	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_194454.3(KRIT1):c.587del (p.Ala196fs)	KRIT1	Likely pathogenic	7	91864859	91864859	AG	A	criteria provided, single submitter	-
single nucleotide variant	NM_194454.3(KRIT1):c.488G>A (p.Trp163Ter)	KRIT1	Likely pathogenic	7	91864958	91864958	C	T	criteria provided, single submitter	-