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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRSS12
(R468*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal recessive 1
GUncertain significance
PRSS12
(G640R)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 1
GUncertain significance
PRSS12
(R757fs)
Indel
(frameshift variant)
Intellectual disability, autosomal recessive 1
GUncertain significance
PRSS12
(W148fs)
Deletion
Intellectual disability, autosomal recessive 1
GLikely pathogenic
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