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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLUD1
(H507Y +2 more)
Single nucleotide variant
(missense variant)
Familial hyperinsulinemia
+1 more
GPathogenic/Likely pathogenic
GLUD1
(S501P +2 more)
Single nucleotide variant
(missense variant)
Hyperinsulinism-hyperammonemia syndrome
GPathogenic
GLUD1
(G499D +2 more)
Single nucleotide variant
(missense variant)
Hyperinsulinism-hyperammonemia syndrome
GPathogenic
GLUD1
(G499S +2 more)
Single nucleotide variant
(missense variant)
Hyperinsulinism-hyperammonemia syndrome
GUncertain significance
GLUD1
(S498L +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
GLUD1
(E349A +2 more)
Single nucleotide variant
(missense variant)
Hyperinsulinism-hyperammonemia syndrome
GPathogenic
GLUD1
(R322H +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
GLUD1
(R318K +2 more)
Single nucleotide variant
(missense variant)
Hyperinsulinism-hyperammonemia syndrome
GUncertain significance
GLUD1
(R274C +2 more)
Single nucleotide variant
(missense variant)
Hyperinsulinism-hyperammonemia syndrome
+1 more
GPathogenic
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