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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CELSR1, LOC121627952
(S2498P)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
CELSR1
(T2155A)
Single nucleotide variant
(missense variant)
Lymphatic malformation 9
GUncertain significance
CELSR1
(G2054C)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
CELSR1
(G1635R)
Single nucleotide variant
(missense variant)
Lymphatic malformation 9
GUncertain significance
CELSR1
(G1424S)
Single nucleotide variant
(missense variant)
Lymphatic malformation 9
GUncertain significance
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