Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Diseases: congenital structural myopathy Molecular Consequence: missense variant
Dnm2tm1.1Ics
(Mus musculus)Allele/Variant
Source: MGI:4848043
Genes: Dnm2 (Mmu)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: centronuclear myopathy
Variant Name: Not Available
Act88FG268D
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0062243
Genes: Act88F (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: congenital structural myopathy
Variant Name: Not Available
Act88FM320
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0038095
Genes: Act88F (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: congenital structural myopathy
Variant Name: Not Available
Act88FR256C
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0248514
Genes: Act88F (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: congenital structural myopathy
Variant Name: Not Available