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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGXT
(T9N)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
AGXT
(P11L)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
AGXT
(N22S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
AGXT
(R118C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
AGXT
(F152I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
AGXT
(G170R)
Single nucleotide variant
(missense variant)
AGXT-related condition
+3 more
GPathogenic/Likely pathogenic
AGXT
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance
AGXT
(A186V)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
AGXT
(R197Q)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
AGXT
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
AGXT
(I279T)
Single nucleotide variant
(missense variant)
AGXT-related condition
+3 more
GConflicting classifications of pathogenicity
AGXT
(R289H)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
AGXT
(I340M)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
AGXT
(E371K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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