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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC39A4
Single nucleotide variant
(intron variant)
Hereditary acrodermatitis enteropathica
+1 more
GBenign
SLC39A4
(T357A +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
+2 more
GBenign
SLC39A4
Single nucleotide variant
(no sequence alteration)
Hereditary acrodermatitis enteropathica
+2 more
GBenign
SLC39A4
(S178C +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
+1 more
GBenign
SLC39A4
(A114T +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary acrodermatitis enteropathica
+2 more
GBenign
SLC39A4
Single nucleotide variant
(synonymous variant +1 more)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(P86L +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(P84L +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary acrodermatitis enteropathica
+2 more
GBenign/Likely benign
SLC39A4
(E10A)
Single nucleotide variant
(missense variant +1 more)
Hereditary acrodermatitis enteropathica
+1 more
GBenign
SLC39A4
(A58T)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
+2 more
GBenign
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
+1 more
GBenign/Likely benign
SLC39A4
Single nucleotide variant
(5 prime UTR variant)
Hereditary acrodermatitis enteropathica
+1 more
GBenign
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