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Links from OMIM

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASTN2, TRIM32
(R394H)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
ASTN2, TRIM32
(C521fs)
Deletion
(frameshift variant +1 more)
Sarcotubular myopathy
+3 more
GPathogenic/Likely pathogenic
ASTN2, TRIM32
(D487N)
Single nucleotide variant
(missense variant +1 more)
Sarcotubular myopathy
+4 more
GPathogenic
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