C4015395[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 586687	NM_052874.5(STX1B):c.840A>G (p.Ser280=)	STX1B	Single nucleotide variant (synonymous variant)	Generalized epilepsy with febrile seizures plus, type 9 +3 more	GBenign
Select item 586685	NM_052874.5(STX1B):c.538-7A>G	STX1B	Single nucleotide variant (intron variant)	Generalized epilepsy with febrile seizures plus, type 9 +3 more	GBenign
Select item 1283427	NM_052874.5(STX1B):c.105+37C>A	STX1B	Single nucleotide variant (intron variant)	Generalized epilepsy with febrile seizures plus, type 9 +2 more	GBenign

Format

Sort by

Choose Destination

ClinVar