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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126862575, MAP3K14
+1 more
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
MAP3K14
(V516I)
Single nucleotide variant
(missense variant)
NIK deficiency
GLikely benign
MAP3K14
Single nucleotide variant
(intron variant)
NIK deficiency
GBenign
MAP3K14
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
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