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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UBL7
(G378R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(P329L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(P284L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(R218W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(A240T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
UBL7
(H234Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(I195V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(A119T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(P123L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(D117E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(D117H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(R24P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(I62V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBL7
(S4P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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