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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2C
(N2848fs)
Deletion
(frameshift variant)
Kleefstra syndrome 1
+2 more
GPathogenic
EHMT1
(G37D +1 more)
Single nucleotide variant
(missense variant)
Kleefstra syndrome 1
GConflicting classifications of pathogenicity
EHMT1
(A100fs +1 more)
Deletion
(frameshift variant)
Kleefstra syndrome 1
GPathogenic
EHMT1
(F222fs +1 more)
Duplication
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
EHMT1
(R260* +2 more)
Single nucleotide variant
(nonsense)
Kleefstra syndrome 1
GPathogenic
EHMT1
(E354fs +2 more)
Microsatellite
(frameshift variant)
Kleefstra syndrome 1
+1 more
GPathogenic
EHMT1
(P440L +2 more)
Single nucleotide variant
(missense variant)
Kleefstra syndrome 1
GConflicting classifications of pathogenicity
EHMT1
(Y529C +2 more)
Single nucleotide variant
(missense variant)
Kleefstra syndrome 1
GUncertain significance
EHMT1
(L711fs +2 more)
Deletion
(frameshift variant)
Kleefstra syndrome 1
GPathogenic
EHMT1
(A772T +2 more)
Single nucleotide variant
(missense variant)
Kleefstra syndrome 1
+1 more
GUncertain significance
EHMT1
(G839V +1 more)
Single nucleotide variant
(missense variant)
Kleefstra syndrome 1
GLikely pathogenic
EHMT1
(D1001fs +1 more)
Deletion
(frameshift variant)
Kleefstra syndrome 1
GPathogenic
EHMT1
(G1285R +1 more)
Single nucleotide variant
(missense variant)
Kleefstra syndrome 1
GConflicting classifications of pathogenicity
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