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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP135
(V213A)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
CEP135
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GConflicting classifications of pathogenicity
CEP135
(I769L)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
CEP135
(S997L)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
CEP135
(R1077Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CEP135
(L1089I)
Single nucleotide variant
(missense variant)
CEP135-related condition
+2 more
GConflicting classifications of pathogenicity
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