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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAST, LOC101929710
+1 more
(S690T +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
CAST, LOC101929710
+1 more
(Q665E +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
CAST, LOC101929710
+1 more
(G226R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CAST, LOC101929710
+1 more
(N221D +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
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