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Items: 59

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCAF8
(N121S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(S200N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(V207M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(N235S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(A189E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(E379D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P424S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(N427S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(I432T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R450Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R452H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R492Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R438K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R444W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P532S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(V588A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P689A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(V715M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P744R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(V747M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P705S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(T772K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(S800N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(S749Y +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(A750T +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SCAF8
(S821L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(I919V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(I876T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P901A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(G904A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(Q951R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(L911S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R1005H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(G1002R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R1028W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P1000L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P1030L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(V1072I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(L1048H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P1096S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(D1103Y +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R1051W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R1051G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(D1124N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(H1156D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R1147G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(E1103A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(Y1206H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P1132T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(G1180S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(H1224R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(R1218H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(W1232S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(F1196S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(H1267Y +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(Q1290H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(P1270S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(V1254D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SCAF8
(I1302L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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