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Items: 1 to 100 of 101

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDHR5
(G645S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A634V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A634T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A614V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A614T +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDHR5
(V609M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(E794Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A596V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(G780S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R783Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(T772K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(G575R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A764V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(G751S +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDHR5
(P561S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A739V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(D735V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(H728P +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDHR5
(V723I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A533V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A717V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(N521K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(C507W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A671V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R468C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(E659D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(S652L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(P645S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(T620P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(M607I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(P606L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(P591L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(P588A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(S579R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(S579G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CDHR5
(P575L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(T553A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(G548A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(Q549R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(S548F +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(G540A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(A527G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(T522I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(N520Y +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(T511K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(T502I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(P485H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(P485A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(P478S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(T471I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(P467H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(T464K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(P463Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDHR5
(I447T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A430T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(T419N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(S407L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A398T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(S393L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(V373A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R360H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R353H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(P351A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A347V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(L332P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(D331N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(M319I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(V315I)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDHR5
(L309F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(N308D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CDHR5
(G282S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(G272R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R270C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(T259M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(V257A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A230T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(T218I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R206Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(L204P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(M199V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R196W)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDHR5
(E195K)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDHR5
(R189Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDHR5
(R182H)
Single nucleotide variant
(missense variant)
not provided
GBenign
CDHR5
(N181S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(F175V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(A171T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R154H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(Q148H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(P145L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(V133A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(V112M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(Q77K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(R72Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(P68H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(G63A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(V54I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(D51Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDHR5
(I36M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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