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Items: 63

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EEF1D
(A276T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
Single nucleotide variant
(splice donor variant)
Inborn genetic diseases
GUncertain significance
EEF1D
(T240S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(V217M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(R195H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(R195C +3 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
EEF1D
(D207G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(K179E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(P171A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(R151Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(A537V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(E143D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(E126Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(P129L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(R117H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(V108I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(R104W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(S119L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(V95M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(L112V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EEF1D
(R71C +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(S452I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(R48C +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(D20N +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
EEF1D
(G351A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(R336W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(H330Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(D323N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(Y322S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(R293W)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
EEF1D
(R292Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(L291P)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
EEF1D
(R281H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(R275H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(R272W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(R264Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(P256T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(P255L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(P255S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(R230Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(A227S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(D207N)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
EEF1D
(Q201H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(P197A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(P188R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(A183S)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
EEF1D
(V159A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(V159M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(D131Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(E122K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(F118S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(F118V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(V111L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(L103F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(D100G)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
EEF1D
(G97S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(G95R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(A63T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(E45K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(A37T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(E31K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(R26H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EEF1D
(D16E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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