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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CPLANE1
(T2995I +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
CPLANE1
(L1279fs)
Microsatellite
(frameshift variant)
Orofaciodigital syndrome type 6
GLikely pathogenic
CPLANE1
(R785*)
Single nucleotide variant
(nonsense)
Joubert syndrome 17
+1 more
GPathogenic
CPLANE1
(T323M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CPLANE1
Single nucleotide variant
(splice donor variant)
Joubert syndrome 17
GLikely pathogenic
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