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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNPAT
(S245C +1 more)
Single nucleotide variant
(missense variant)
Rhizomelic chondrodysplasia punctata type 2
+1 more
GUncertain significance
GNPAT
(D330Y +1 more)
Single nucleotide variant
(missense variant)
Rhizomelic chondrodysplasia punctata type 2
+1 more
GUncertain significance
GNPAT
(R344Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
GNPAT
Single nucleotide variant
(intron variant)
Rhizomelic chondrodysplasia punctata type 2
+1 more
GBenign/Likely benign
GNPAT
(D519G +1 more)
Single nucleotide variant
(missense variant)
Rhizomelic chondrodysplasia punctata type 2
+2 more
GBenign/Likely benign
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