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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2D
Single nucleotide variant
(intron variant)
Kabuki syndrome
+3 more
GConflicting classifications of pathogenicity
KMT2D
(Q4859*)
Single nucleotide variant
(nonsense)
Kabuki syndrome 1
GPathogenic
KMT2D
(E4718K)
Single nucleotide variant
(missense variant)
Kabuki syndrome 1
GUncertain significance
KMT2D
(T4668S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KMT2D
(A3552fs)
Insertion
(frameshift variant)
Kabuki syndrome 1
GLikely pathogenic
KMT2D
(Q2811fs)
Duplication
(frameshift variant)
Kabuki syndrome 1
GPathogenic
KMT2D
(T2203S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
KMT2D
(R1709fs)
Microsatellite
(frameshift variant)
not provided
+2 more
GPathogenic/Likely pathogenic
KMT2D
(M1530I)
Single nucleotide variant
(missense variant)
Kabuki syndrome 1
GUncertain significance
KMT2D
(P1131L)
Single nucleotide variant
(missense variant)
KMT2D-related condition
+3 more
GConflicting classifications of pathogenicity
KMT2D
(P638A)
Single nucleotide variant
(missense variant)
Kabuki syndrome 1
+2 more
GConflicting classifications of pathogenicity
KMT2D
(S543L)
Single nucleotide variant
(missense variant)
Kabuki syndrome 1
+1 more
GConflicting classifications of pathogenicity
KMT2D
(K287*)
Duplication
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
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