"Ambry Genetics"[submitter] AND "GAL"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 574523	NM_015973.5(GAL):c.43G>A (p.Ala15Thr)	GAL (A15T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 571157	NM_015973.5(GAL):c.178C>T (p.Leu60Phe)	GAL (L60F)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 542524	NM_015973.5(GAL):c.199C>T (p.Arg67Trp)	GAL (R67W)	Single nucleotide variant (missense variant)	Familial temporal lobe epilepsy 8 +1 more	GUncertain significance
Select item 475911	NM_015973.5(GAL):c.205G>A (p.Glu69Lys)	GAL (E69K)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3097982	NM_015973.5(GAL):c.214A>G (p.Met72Val)	GAL (M72V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 475912	NM_015973.5(GAL):c.263G>A (p.Arg88His)	GAL (R88H)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 983369	NM_015973.5(GAL):c.316G>C (p.Asp106His)	GAL (D106H)	Single nucleotide variant (missense variant)	Seizure +1 more	GUncertain significance
Select item 940511	NM_015973.5(GAL):c.368C>T (p.Ser123Phe)	GAL (S123F)	Single nucleotide variant (missense variant)	Familial temporal lobe epilepsy 8 +1 more	GUncertain significance

ClinVar