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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMT
(A361V +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
AMT
(R73C)
Single nucleotide variant
(missense variant +2 more)
See cases
+2 more
GPathogenic/Likely pathogenic
GLDC
(A794fs)
Deletion
(frameshift variant)
Non-ketotic hyperglycinemia
GPathogenic/Likely pathogenic
GLDC
(R59T)
Single nucleotide variant
(missense variant)
Non-ketotic hyperglycinemia
+1 more
GConflicting classifications of pathogenicity
GCSH, LOC130059495
(R17C)
Single nucleotide variant
(missense variant +1 more)
Non-ketotic hyperglycinemia
GUncertain significance
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