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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPG5
Single nucleotide variant
(intron variant)
Vici syndrome
GUncertain significance
EPG5
(V1133L)
Single nucleotide variant
(missense variant)
Vici syndrome
GUncertain significance
EPG5
(T1005M)
Single nucleotide variant
(missense variant)
Vici syndrome
GUncertain significance
EPG5
(Q336R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
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