"Genome-Nilou Lab"[submitter] AND "SLC2A1-DT"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1686206	NM_006516.4(SLC2A1):c.1A>G (p.Met1Val)	SLC2A1, SLC2A1-DT (M1V)	Single nucleotide variant (missense variant +1 more)	Encephalopathy due to GLUT1 deficiency +1 more	GPathogenic
Select item 297395	NM_006516.2(SLC2A1):c.-490G>C	SLC2A1, SLC2A1-DT	Single nucleotide variant (non-coding transcript variant)	Encephalopathy due to GLUT1 deficiency +7 more	GBenign