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Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRCC
(E20D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P21A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P33S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P52S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P75T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(N121S)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
PRCC
(H153D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P201R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P208H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(S209L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(D214H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(K225N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(G234V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P240L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(E274K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(L279F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P286A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P333R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(D341G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(P379A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC120893163, PRCC
(S420I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC120893163, PRCC
(M436V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRCC
(R467Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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