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Items: 83

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC39A4
Single nucleotide variant
(3 prime UTR variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(3 prime UTR variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(E144K +3 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(R115W +3 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SLC39A4
(V485L +3 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
LOC130001397, SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC130001397, SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC130001397, SLC39A4
(A12G +3 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(D504G +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(M499V +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign
SLC39A4
(E383K +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(E476K +1 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary acrodermatitis enteropathica
+2 more
GUncertain significance
SLC39A4
(E476Q +1 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(R445H +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(P462S +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(S346T +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(D402H +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SLC39A4
(A412T +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(G409R +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(E392Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(V384M +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(intron variant)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(T381A +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
SLC39A4
(A376T +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(no sequence alteration)
not provided
+1 more
GBenign
SLC39A4
(T357A +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
+2 more
GBenign
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(A247V +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
SLC39A4
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
SLC39A4
(P290L +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(E284K +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
SLC39A4
(S258L +2 more)
Single nucleotide variant
(missense variant)
SLC39A4-related condition
+2 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
SLC39A4
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(T268M +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(E191K +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(A198T +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(G155S +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(S178C +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
SLC39A4
(A148V +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
+2 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(A76V +2 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
+1 more
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
SLC39A4
Single nucleotide variant
(no sequence alteration)
not provided
+1 more
GBenign
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(Q120H +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(H122Y +1 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(A114T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign
SLC39A4
(V101I +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary acrodermatitis enteropathica
+2 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(V93I +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant)
Hereditary acrodermatitis enteropathica
+1 more
GBenign
SLC39A4
(P86L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(P84L +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GBenign/Likely benign
SLC39A4
(G54R +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(C37S)
Single nucleotide variant
(missense variant +1 more)
Hereditary acrodermatitis enteropathica
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
SLC39A4
(A58T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC39A4
(G35A)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
SLC39A4
Single nucleotide variant
(5 prime UTR variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
(5 prime UTR variant)
Hereditary acrodermatitis enteropathica
GBenign
SLC39A4
Single nucleotide variant
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
Single nucleotide variant
Hereditary acrodermatitis enteropathica
GLikely benign
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