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Links from Gene

Items: 43

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RANBP3-DT, RFX2
(K660T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(E396K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(V504I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(D326E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(P603L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(A343T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(A651T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R201Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(L294V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(P298L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(G318S +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RANBP3-DT, RFX2
(G314V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(G289S +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RANBP3-DT, RFX2
(M288V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(T285M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R280Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(L215I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(A560V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(D515N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
RANBP3-DT, RFX2
(L395V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R525Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(C411W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(S590I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(N376D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(E691K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R566Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R350W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(H718Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R688H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(P465L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R693H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(A672V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(G409S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(F216L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R512P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(R677H +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RANBP3-DT, RFX2
(T568I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(T469I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(D659N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(D408H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(E353K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RANBP3-DT, RFX2
(I449T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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