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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TULP1
Single nucleotide variant
(splice donor variant)
not provided
+3 more
GPathogenic
TULP1
(R429Q +1 more)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 14
+1 more
GPathogenic
TULP1
Single nucleotide variant
(intron variant)
Leber congenital amaurosis 15
GUncertain significance
TULP1
(R311W +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
TULP1
(E117K)
Single nucleotide variant
(missense variant +1 more)
Retinitis pigmentosa 14
+1 more
GConflicting classifications of pathogenicity
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