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Items: 77

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNTROB
(G13R)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CNTROB
(G13E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(G26R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(Q29K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(S31L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(T35N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(A48G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(R53G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(H65R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(G67R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(G70S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(A72T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(R103Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(R17* +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
CNTROB
(R131Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(L145P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(Y169H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(P180H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(R107H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(L125I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CNTROB
(T230I +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CNTROB
(M142I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R152H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(H175Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R191H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(N107S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R205H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(S209N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R326W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R334Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R257Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R166Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CNTROB
(A375V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(E193D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(A212T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R227W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R237G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R444Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(S449P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R373Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(D398N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(H306Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(H306Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(A322V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(V532M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R360W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(Q380K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(P387L +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CNTROB
(A490V +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CNTROB
(P398L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(E405A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(W414C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(E436K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(C445F +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(L451V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(S477Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(F488L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(G604R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CNTROB
(P548A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(P755L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R683W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(E775A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R728W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(L834V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(S651R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(G856E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(P781S +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R782H +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(R783C +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CNTROB
(R685H +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
CNTROB
(A697T +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CNTROB
(R906Q +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(R898W +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CNTROB
(G900E +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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