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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP7A
(R123K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
ATP7A
(I189V)
Single nucleotide variant
(missense variant)
not specified
+5 more
GBenign/Likely benign
ATP7A
(L520F)
Single nucleotide variant
(missense variant)
X-linked distal spinal muscular atrophy type 3
+3 more
GConflicting classifications of pathogenicity
ATP7A
(Q704R)
Single nucleotide variant
(missense variant)
X-linked distal spinal muscular atrophy type 3
+2 more
GBenign/Likely benign
ATP7A
(R844C +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GBenign/Likely benign
ATP7A
(I1024V +1 more)
Single nucleotide variant
(missense variant)
Menkes kinky-hair syndrome
+2 more
GUncertain significance
ATP7A
Single nucleotide variant
(synonymous variant +1 more)
Menkes kinky-hair syndrome
+2 more
GLikely benign
ATP7A
(V1401L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+5 more
GBenign/Likely benign
ATP7A
(L1452F +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
ATP7A
(I1464V +1 more)
Single nucleotide variant
(missense variant +1 more)
Ehlers-Danlos syndrome
+5 more
GBenign
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