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Items: 55

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RGL2
(G760V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(G678D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(I711L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(Y615H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R689C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(V601A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R682H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(D661G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(G551R +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RGL2
(G627V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R612G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(P598L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R569Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R487W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(G556A +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RGL2
(R469W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(P463L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(P463R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(T462I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R443Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R522Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(A520G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R414Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RGL2
(P402S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(V466I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R342W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(H332Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(V320M +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RGL2
(N311S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(W288L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(V273L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(V354M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R346Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R255H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R248W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(P326R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(G217R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(A216V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(S199C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(P236T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(D134N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(S213F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R209H +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RGL2
(G120V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(G202W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(G201E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(G201V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RGL2
(G197R +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RGL2
(E151K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(M55T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(A119V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(R90Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RGL2
(G41A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
RGL2
(D27N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
RGL2
(S13R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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