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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRPF4
(P186A +1 more)
Single nucleotide variant
(missense variant +2 more)
Retinal dystrophy
GUncertain significance
PRPF4
(A248V +1 more)
Single nucleotide variant
(missense variant +2 more)
Retinal dystrophy
GUncertain significance
PRPF4
(T323I +2 more)
Single nucleotide variant
(missense variant +1 more)
Retinal dystrophy
+1 more
GUncertain significance
PRPF4
Single nucleotide variant
(intron variant)
Retinal dystrophy
GUncertain significance
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