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Items: 16

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CX3CR1
(S327F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(S327T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(R318C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(S284G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(T310A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(L290F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(T245I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(W276C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(V189M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(L183F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(G209S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(A162G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(A194V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(D126Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(F119S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CX3CR1
(N131S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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