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Items: 63

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
YEATS2
(D12N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(E31K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(Q40R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(S96F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(A111G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(S157N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(N158S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(R183G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(G186A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(H188L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(Q192R)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
YEATS2
(R193Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(R242C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(R242H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(F257V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(V287I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(I359T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(V363L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(P368S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(R478Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(T514I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(T527M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(H542Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(I591V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(A603T +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
YEATS2
(S609R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(A643E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(Q733R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(G815S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(G818R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(G819S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(G828R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(T857I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(Q875H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(L886V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(L939V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(S939L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(L947R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(T957I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(V961M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(T987M +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
YEATS2
(S990T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(A1008P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(V1014I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
YEATS2
(T1016M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(V1019M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(N1023D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(L1058P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(T1063I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(A1107G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(L1121V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(L1121P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(S1176F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(K1203N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(H1217R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(I1226V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(S1250F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(K1310E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2
(F1320L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
YEATS2, YEATS2-AS1
(T1341I +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
YEATS2, YEATS2-AS1
(V1345M +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
YEATS2, YEATS2-AS1
(R1350K +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GLikely benign
LOC126806889, YEATS2
(I1388V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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