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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RFT1
(N385S)
Single nucleotide variant
(missense variant)
RFT1-congenital disorder of glycosylation
GConflicting classifications of pathogenicity
RFT1
(R373C)
Single nucleotide variant
(missense variant)
RFT1-congenital disorder of glycosylation
GUncertain significance
RFT1
(D274G)
Single nucleotide variant
(missense variant)
RFT1-congenital disorder of glycosylation
GConflicting classifications of pathogenicity
RFT1
(R261G)
Single nucleotide variant
(missense variant)
RFT1-congenital disorder of glycosylation
GUncertain significance
APEH, HEMK1
+177 more
Copy number gain
not provided
GPathogenic
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