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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSNK2A1
(P227H +1 more)
Single nucleotide variant
(missense variant)
Okur-Chung neurodevelopmental syndrome
GUncertain significance
CSNK2A1
(S356T +1 more)
Single nucleotide variant
(missense variant)
Okur-Chung neurodevelopmental syndrome
+1 more
GUncertain significance
CSNK2A1
(K198R +1 more)
Single nucleotide variant
(missense variant)
Okur-Chung neurodevelopmental syndrome
+4 more
GPathogenic/Likely pathogenic
CSNK2A1
(N161D +1 more)
Single nucleotide variant
(missense variant)
Okur-Chung neurodevelopmental syndrome
GLikely pathogenic
CSNK2A1
(Q126fs)
Deletion
(frameshift variant +1 more)
Okur-Chung neurodevelopmental syndrome
GPathogenic
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