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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130009662, TNFSF11
(E27G)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign
LOC130009662, TNFSF11
(G28D)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
LOC130009662, TNFSF11
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign
LOC130009662, TNFSF11
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign
TNFSF11
(A72T)
Single nucleotide variant
(missense variant +1 more)
TNFSF11-related condition
+2 more
GConflicting classifications of pathogenicity
TNFSF11, LOC126861752
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
LOC126861753, TNFSF11
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
TNFSF11
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TNFSF11
(R211Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TNFSF11
(V240I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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