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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129934738, SAP130
(G19R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129934738, SAP130
(A14G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129934738, SAP130
(P7S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129934738, SAP130
(P3L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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