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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130058985, TENT4B
(G99A +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LOC130058985, TENT4B
(P135L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130058985, TENT4B
(S143G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130058985, TENT4B
(Y174H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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