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Links from Gene

Items: 41

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC183, CCDC183-AS1
(L413F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(D436Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(A348T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(N274K)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(S432F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(L332P)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(R311Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GLikely benign
CCDC183, CCDC183-AS1
(V306A)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(T255R)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, LOC130003039
(I168V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(D504N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(V455M)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(Q296*)
Single nucleotide variant
(non-coding transcript variant +1 more)
See cases
GLikely pathogenic
CCDC183, CCDC183-AS1
(V299M)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(G524R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(T483I)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(R363L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(G419D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(R490W)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(R223S)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(T255M)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(R237Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(D411N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(K248Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(E229K)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(S308N)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(S367C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(E304K)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(E260K)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(E304Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(S273L)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(R416Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(N421D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(S394G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(D268E)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, LOC130003039
(L173F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(T328M)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(I253T)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CCDC183, CCDC183-AS1
(H393Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CCDC183, CCDC183-AS1
(A424E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC183-AS1, CCDC183
(W342*)
Single nucleotide variant
(nonsense)
Essential tremor
GLikely pathogenic
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