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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TULP1
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign
TULP1
(K261N +1 more)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+6 more
GBenign
TULP1
(I259T +1 more)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis 15
+6 more
GBenign
TULP1
Single nucleotide variant
(intron variant)
Leber congenital amaurosis 15
+2 more
GBenign
TULP1
(T67R)
Single nucleotide variant
(missense variant +1 more)
Leber congenital amaurosis 15
+5 more
GBenign
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