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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SZT2
(R25*)
Single nucleotide variant
(nonsense)
Developmental and epileptic encephalopathy, 18
GPathogenic
SZT2
(S499I)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 18
GPathogenic
SZT2
(Q698*)
Single nucleotide variant
(nonsense)
Developmental and epileptic encephalopathy, 18
GPathogenic
SZT2
Single nucleotide variant
(splice donor variant)
not provided
GPathogenic
SZT2
(A1167fs +1 more)
Duplication
(frameshift variant)
Developmental and epileptic encephalopathy, 18
GPathogenic
SZT2
(N1234fs +1 more)
Deletion
(frameshift variant)
Developmental and epileptic encephalopathy, 18
GPathogenic
SZT2
(F1401del +1 more)
Microsatellite
(inframe_deletion)
not provided
GConflicting classifications of pathogenicity
SZT2
(G1829fs +1 more)
Deletion
(frameshift variant)
Developmental and epileptic encephalopathy, 18
GPathogenic
SZT2
(R2185W +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
SZT2
(R2435W +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SZT2
(C2481Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SZT2
(W2609G +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 18
GPathogenic
SZT2
(S2721C +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 18
GPathogenic
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