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Items: 59

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LGR4
(R941H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(A905V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(V899L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(A880D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(P892H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(C857G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(D835N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(D859H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(V833I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(G846S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(A770P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(P767Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(V723I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LGR4
(T677M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(P691S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(E686K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(G672A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(N633T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(S592G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(G591S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(T571S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(L519V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(G537E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(T485I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(T476I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(H468Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(N483I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(T406M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(T402N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(R383G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(I365V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(T384I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(R350C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(R356G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(R346S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(K330E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(T329A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(S323R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(Q287H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(Q310R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(D297G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(A291T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(N289I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(P259R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(S257G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(T166M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(G103R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(R102Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(R102P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4
(S98R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
(A61V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
(P52L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
(D42H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
+1 more
(A30S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
+1 more
(P27S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
+1 more
(G20E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
+1 more
(S18L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
+1 more
(G17C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LGR4, LGR4-AS1
+1 more
(L16R)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
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