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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EIF2B5
(R113H)
Single nucleotide variant
(missense variant)
See cases
+4 more
GPathogenic
EIF2B5
(R136H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
EIF2B5
(G297S)
Single nucleotide variant
(missense variant)
Vanishing white matter disease
GPathogenic
EIF2B5
(M305L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
EIF2B5
(R344G)
Single nucleotide variant
(missense variant)
Vanishing white matter disease
GLikely pathogenic
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