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Items: 40

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACSBG2, LOC105372255
(G3E)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ACSBG2, LOC105372255
(V23G)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(R32Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(D33G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(G44R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(Y37H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(F119L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(E142K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(S174R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(A180V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACSBG2, LOC105372255
(K140N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(E30K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(T248M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(V254L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(I89T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(H141Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(A149P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(A336T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(S338T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(V160M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(G367R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(G256V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(L259W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(L259F +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(S291T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(T482I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(S307C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(G510S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(E327G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(P475L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(I527T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(A356T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(M544T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(T508M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(D550V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(Q580H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(N571D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(D447E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACSBG2, LOC105372255
(M617T +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ACSBG2, LOC105372255
(I661T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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