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Items: 53

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DENND1C
(G757D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R789Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
DENND1C
(R789W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(T778N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R765W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(P752H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R750W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(P663T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(P657T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(T656A +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
DENND1C
(R639S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(S594A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(S619C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(D548E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(A530T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
DENND1C
(M525T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(W497G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R471C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(I455V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R448H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R448G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(G435D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(V418M +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
DENND1C
(A411V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(A374S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(G369R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(G356D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R347Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(E389Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(Q386R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(A329S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(S358N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(P307R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(N249S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(A292T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R234G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(G181R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(P119R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(P163H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(I161T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(G114R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(T110M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(T110K +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
DENND1C
(P97S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(L67F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(G78D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(H24N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(A21T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(S19G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DENND1C
(R33Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DENND1C
(S9F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DENND1C
(G8C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DENND1C
(S3F)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
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