動脈蛇行症候群

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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_030777.4(SLC2A10):c.1288+2T>C	SLC2A10	Likely pathogenic	20	45354965	45354965	T	C	criteria provided, single submitter	-
Deletion	NC_000020.11:g.(?_46709717)_(46733854_?)del	SLC2A10	Pathogenic	20	45338356	45362493	na	na	criteria provided, single submitter	-
single nucleotide variant	NM_030777.4(SLC2A10):c.395G>T (p.Arg132Leu)	SLC2A10	Likely pathogenic	20	45354070	45354070	G	T	criteria provided, single submitter	ClinGen:CA409266928
single nucleotide variant	NM_030777.4(SLC2A10):c.648C>G (p.Tyr216Ter)	SLC2A10	Pathogenic/Likely pathogenic	20	45354323	45354323	C	G	criteria provided, multiple submitters, no conflicts	ClinGen:CA315755913
Indel	NM_030777.4(SLC2A10):c.1278_1287delinsCC (p.Phe427fs)	SLC2A10	Pathogenic	20	45354953	45354962	GTTTGGGCCA	CC	criteria provided, single submitter	ClinGen:CA16620930
single nucleotide variant	NM_030777.4(SLC2A10):c.1411+2T>A	SLC2A10	Likely pathogenic	20	45355627	45355627	T	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA322146
single nucleotide variant	NM_030777.4(SLC2A10):c.1330C>T (p.Arg444Ter)	SLC2A10	Pathogenic/Likely pathogenic	20	45355544	45355544	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA347799
single nucleotide variant	NM_030777.4(SLC2A10):c.1309G>A (p.Glu437Lys)	SLC2A10	Pathogenic/Likely pathogenic	20	45355523	45355523	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA347770,UniProtKB:O95528#VAR_042423
Deletion	NM_030777.4(SLC2A10):c.731_734del (p.Leu244fs)	SLC2A10	Pathogenic	20	45354403	45354406	CAACT	C	criteria provided, multiple submitters, no conflicts	ClinGen:CA347754
single nucleotide variant	NM_030777.4(SLC2A10):c.691C>T (p.Arg231Trp)	SLC2A10	Pathogenic/Likely pathogenic	20	45354366	45354366	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA319966