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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRODH
(F488L +1 more)
Single nucleotide variant
(missense variant)
Proline dehydrogenase deficiency
GUncertain significance
PRODH
(Q418* +1 more)
Single nucleotide variant
(nonsense)
Schizophrenia 4
+2 more
GUncertain significance
PRODH
(L441P +1 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
PRODH
(M204V +1 more)
Single nucleotide variant
(missense variant)
Proline dehydrogenase deficiency
GUncertain significance
PRODH
Single nucleotide variant
(intron variant)
Proline dehydrogenase deficiency
GConflicting classifications of pathogenicity
PRODH
(G193D +1 more)
Single nucleotide variant
(missense variant)
Proline dehydrogenase deficiency
+2 more
GUncertain significance
PRODH
(S162Y +1 more)
Single nucleotide variant
(missense variant)
Proline dehydrogenase deficiency
GUncertain significance
PRODH
(D143Y +1 more)
Single nucleotide variant
(missense variant)
Proline dehydrogenase deficiency
GUncertain significance
PRODH
(P8S)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
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