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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAPN15
(G19C)
Single nucleotide variant
(missense variant)
Oculogastrointestinal-neurodevelopmental syndrome
GUncertain significance
CAPN15
(R736*)
Single nucleotide variant
(nonsense)
Oculogastrointestinal-neurodevelopmental syndrome
GLikely pathogenic
CAPN15
(V841M)
Single nucleotide variant
(missense variant)
Oculogastrointestinal-neurodevelopmental syndrome
GUncertain significance
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