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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TFG
(L97P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TFG
(R106H)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 57
+4 more
GConflicting classifications of pathogenicity
TFG
(S183P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TFG
(A184T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
TFG
(P304S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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