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Items: 66

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNTN5
(M8K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CNTN5
(S65Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTN5
(W69G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTN5
(W69C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTN5
(A72E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTN5
(A46E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R126H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(P129S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(G81D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(I85V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(S110N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(P146Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(N203D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(M295L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(H231Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(P254S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R272H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R274Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(L280M +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
CNTN5
(N358K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(V319L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(T399I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R344I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(Y347H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(M364I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(M370I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(P431S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(I439V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(A521E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R537Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(E546Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(G479V +1 more)
Single nucleotide variant
(missense variant)
CNTN5-related disorder
+1 more
GConflicting classifications of pathogenicity
CNTN5
(I489L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(I540V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(E543K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(G547R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(S631A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(G672D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(E684K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R635C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(E650K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(S658P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R767C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(T768A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(I792M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(E726G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R819H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(R763Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(P846L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(P772R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(A797P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(A810V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(S859Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(H947D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(S889G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(S898Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(P899S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(S905G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(W909C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(A1001G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(E929V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(G943V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(P1034S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(G965E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(G1067D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTN5
(S1010L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
Display optionsSort by LocationDownload
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