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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CD3D
(R125W +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CD3D
(E129G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GUncertain significance
CD3D
(V86M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CD3D
(I70M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
CD3D
(R63H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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