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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WASHC5
(N836D +1 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 8
GUncertain significance
WASHC5
(H575R +1 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 8
GUncertain significance
WASHC5
(M1T)
Single nucleotide variant
(missense variant +2 more)
Hereditary spastic paraplegia 8
GUncertain significance
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