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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TET3
(T851M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
TET3
(E780K +1 more)
Single nucleotide variant
(missense variant)
Beck-Fahrner syndrome
GUncertain significance
TET3
(K1003fs +1 more)
Deletion
(frameshift variant)
Beck-Fahrner syndrome
GLikely pathogenic
TET3
(S1352Y +1 more)
Single nucleotide variant
(missense variant)
Beck-Fahrner syndrome
GUncertain significance
TET3
(R1548C +2 more)
Single nucleotide variant
(missense variant)
Beck-Fahrner syndrome
GUncertain significance
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