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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDK10, LINC02166
Single nucleotide variant
(non-coding transcript variant +2 more)
Al Kaissi syndrome
+1 more
GConflicting classifications of pathogenicity
CDK10
(R57W)
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
+2 more
GUncertain significance
CDK10
(T88R +1 more)
Single nucleotide variant
(missense variant +1 more)
Al Kaissi syndrome
GUncertain significance
CDK10
(V28L +1 more)
Single nucleotide variant
(missense variant +1 more)
Al Kaissi syndrome
GUncertain significance
CDK10
(C105S +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
CDK10
(D150N +1 more)
Single nucleotide variant
(missense variant +1 more)
Al Kaissi syndrome
+1 more
GUncertain significance
CDK10
(I228M +1 more)
Single nucleotide variant
(missense variant +1 more)
Al Kaissi syndrome
GUncertain significance
CDK10
(S278R +2 more)
Single nucleotide variant
(missense variant +2 more)
Al Kaissi syndrome
GUncertain significance
ACSF3, ADAD2
+83 more
Copy number gain
not provided
GPathogenic
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