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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NOTCH2
(I2304fs)
Duplication
(frameshift variant)
Hajdu-Cheney syndrome
GPathogenic/Likely pathogenic
FCN1
(G152R)
Single nucleotide variant
(missense variant)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
RAPGEF1
(Y572C +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SP4
(R690W +2 more)
Single nucleotide variant
(missense variant)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
TMED9
(L26Q)
Single nucleotide variant
(missense variant)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
APC
(M702V +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+1 more
GUncertain significance
KLHL6
(F83L)
Single nucleotide variant
(missense variant)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
KLHL6
(L90V)
Single nucleotide variant
(missense variant)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
SLC35A5
(L118R)
Single nucleotide variant
(missense variant +1 more)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
DAZAP1
(Y405H +2 more)
Single nucleotide variant
(missense variant +1 more)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
SEC14L1
(P34A)
Single nucleotide variant
(missense variant +1 more)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
AMZ2
(T174K +3 more)
Single nucleotide variant
(missense variant +1 more)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
VMP1
(L111fs +1 more)
Deletion
(frameshift variant +2 more)
Monoclonal B-Cell Lymphocytosis
GUncertain significance
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