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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXO25
(S42T)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
FBXO25
(K68E)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GUncertain significance
FBXO25
(E96K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FBXO25
(R42Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(F122Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(R167C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(S123C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(E204Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(D215H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(D230E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(R242W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(G246R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(G253C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(K271N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(E223G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(I227T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(H266Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(P267L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(D339E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FBXO25
(I353T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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