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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2A
(K2012* +1 more)
Single nucleotide variant
(nonsense)
not provided
GLikely pathogenic
KMT2A
(R3527Q +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
KMT2A
(R3564W +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
KMT2A
(I3572S +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
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