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Items: 41

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCT
(E455G +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(R514G +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(S448R +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(G405V +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(R428W +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(H363D +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(I424V +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(P446S +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
DCT
(M407I +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(P421L)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(T417A)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(V330M +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(A381T +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(G67W +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(F64L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(N307H +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(A294E +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(S32A +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(N279K +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCT
(G242D +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(D227Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(C223R +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(R278K +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(D268G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(T195I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(R170L +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(H160R +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(R158Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(R158W +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(V154I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(R139C +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(N170T +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
DCT
(S134N +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
DCT
(E119K +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
DCT
(G115S +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
DCT
(G49C +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
DCT
(P87Q)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(R83C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(K38T)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(R27Q)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DCT
(P26L)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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