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Links from Gene

Items: 1 to 100 of 119

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLPX
(G250D)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(S420P)
Single nucleotide variant
(missense variant +1 more)
CLPX-related disorder
GUncertain significance
CLPX
(R51S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(G379D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(S142L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(Q47R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(G254V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(R210G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(A631T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(D583H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(R480C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
Single nucleotide variant
(3 prime UTR variant +1 more)
CLPX-related disorder
GLikely benign
CLPX
(A13T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(V418M)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
(D110E)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(G100R)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
Single nucleotide variant
(intron variant)
not provided
GBenign
CLPX
(E128K)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(L16I)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(E539K)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
CLPX
(T219I)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
(S19A)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CLPX
(S184P)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(R373W)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(R477W)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
(K475R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
(A551D)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
(G10A)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(D458V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(R123H)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(F417L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
CLPX
(T122A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(V14G)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
CLPX
(T43I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(E614G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
(Q352H)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
CLPX
(N344K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(P165S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(I147V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(L16R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(G623E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(A156V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(A531T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(G464E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(R485G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLPX
(E588V)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
CLPX
(S466L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(N424S)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
(V14A)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
(R477Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(T413A)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(T8A)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
(A454V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely benign
CLPX
Duplication
(intron variant)
not provided
GLikely benign
CILP, CLPX
+3 more
Copy number gain
not provided
GUncertain significance
CLPX
Single nucleotide variant
(intron variant)
not provided
GBenign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
(R104C)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
CLPX
(T46I)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
CLPX
(I488T)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
CLPX
Single nucleotide variant
(intron variant)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
CLPX
(R32P)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
CLPX
(G250S)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
CLPX
(E155K)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GConflicting classifications of pathogenicity
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CLPX
(S19F)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
ANKDD1A, CILP
+16 more
Copy number gain
not specified
GUncertain significance
CLPX
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CLPX
(Q162E)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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