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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SKIC3
(Q1487R)
Single nucleotide variant
(missense variant)
Trichohepatoenteric syndrome 1
GUncertain significance
SKIC3
(D1461G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SKIC3
(S1437I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SKIC3
(H709Y)
Single nucleotide variant
(missense variant)
Trichohepatoenteric syndrome 1
+2 more
GUncertain significance
SKIC3
(G578V)
Single nucleotide variant
(missense variant)
Trichohepatoenteric syndrome 1
GUncertain significance
SKIC3
Single nucleotide variant
(synonymous variant)
Trichohepatoenteric syndrome 1
GUncertain significance
SKIC3
(G277S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SKIC3
(R137*)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic/Likely pathogenic
AGK
(R137*)
Single nucleotide variant
(nonsense)
Cataract 38
+3 more
GPathogenic
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