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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
JAG1
(R683H)
Single nucleotide variant
(missense variant)
Alagille syndrome due to a JAG1 point mutation
GLikely benign
JAG1
(I654fs)
Deletion
(frameshift variant)
Alagille syndrome due to a JAG1 point mutation
GPathogenic
JAG1
(Q608fs)
Microsatellite
(frameshift variant)
Alagille syndrome due to a JAG1 point mutation
GLikely pathogenic
JAG1
(N394fs)
Duplication
(frameshift variant)
Alagille syndrome due to a JAG1 point mutation
GPathogenic
JAG1
(S32*)
Single nucleotide variant
(nonsense)
Alagille syndrome due to a JAG1 point mutation
GPathogenic
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