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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASXL2
(V1094A +2 more)
Single nucleotide variant
(missense variant)
Shashi-Pena syndrome
GUncertain significance
ASXL2
(S1074A +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ASXL2
(S1030N +2 more)
Single nucleotide variant
(missense variant)
Shashi-Pena syndrome
GUncertain significance
ASXL2
(R1023C +2 more)
Single nucleotide variant
(missense variant)
Shashi-Pena syndrome
+2 more
GConflicting classifications of pathogenicity
ASXL2
(P1178S +2 more)
Single nucleotide variant
(missense variant)
Shashi-Pena syndrome
GUncertain significance
ASXL2
(N676D +2 more)
Single nucleotide variant
(missense variant)
Shashi-Pena syndrome
GUncertain significance
ASXL2
(R459fs +2 more)
Microsatellite
(frameshift variant)
Shashi-Pena syndrome
GUncertain significance
ASXL2
(S206F +2 more)
Single nucleotide variant
(missense variant)
Shashi-Pena syndrome
GUncertain significance
ASXL2
(L237I +2 more)
Single nucleotide variant
(missense variant)
Shashi-Pena syndrome
GUncertain significance
ASXL2
(K177Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GBenign/Likely benign
ASXL2
(P140L +1 more)
Single nucleotide variant
(missense variant +1 more)
Shashi-Pena syndrome
+1 more
GUncertain significance
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