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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP2A1
Single nucleotide variant
(synonymous variant)
ATP2A1-related condition
+3 more
GConflicting classifications of pathogenicity
ATP2A1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
ATP2A1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
ATP2A1
Deletion
(intron variant)
not specified
+2 more
GBenign/Likely benign
ATP2A1
(N741fs +1 more)
Deletion
(frameshift variant)
Brody myopathy
+1 more
GConflicting classifications of pathogenicity
ATP2A1
(M800fs +1 more)
Duplication
(frameshift variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ATP2A1
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GBenign
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