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Items: 36

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PROSER2, PROSER2-AS1
(S34N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(I108V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(G118R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
PROSER2, PROSER2-AS1
(T146I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(P180A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(R221W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(P228S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(N256S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(R265Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(R265P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(V276A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(Q279R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(R282W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(S311F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(S312F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(P323S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(G324R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(E327G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(L329F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(A331T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(G332R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(R337W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(G338C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(P339S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(P339R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(H349Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(A351S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(L352P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(A373S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(R378W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(R380S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(P386S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2, PROSER2-AS1
(R387W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(A392G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
PROSER2, PROSER2-AS1
(E433G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PROSER2-AS1, PROSER2
(S435T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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