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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNFSF4
(G117S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TNFSF4
(L129V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TNFSF4
(S66N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TNFSF4
(V38M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TNFSF4
(R55Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
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