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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TULP1
(A496T +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
TULP1
(G266V +1 more)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa
+2 more
GUncertain significance
TULP1
Single nucleotide variant
(intron variant)
not specified
+1 more
GUncertain significance
TULP1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
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