Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Genes
Allele/Variant Genes: Calx (Dme)
Calx1
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0362675
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
CalxB
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0193745
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Calxf04627
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0184410
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(R6)3R:20995829A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20995829A>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20995829A>T
(R6)3R:20995841A>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20995841A>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20995841A>C
(R6)3R:20995842A>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20995842A>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20995842A>C
(R6)3R:20987217T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20987217T>C
Genes: CG43446 (Dme), Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20987217T>C
(R6)3R:20987242G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20987242G>A
Genes: CG43446 (Dme), Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20987242G>A
(R6)3R:20987261A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20987261A>G
Genes: CG43446 (Dme), Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20987261A>G
(R6)3R:20990799T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20990799T>A
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20990799T>A
(R6)3R:20991021T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20991021T>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20991021T>C
(R6)3R:20998689T>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20998689T>G
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20998689T>G
(R6)3R:20998800A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20998800A>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20998800A>T
CalxC
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0193746
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
CalxE
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0193748
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
CalxA
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0193744
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
CalxMI09964
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0290831
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3R:20978648G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20978648G>A
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20978648G>A
(R6)3R:20978656A>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20978656A>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20978656A>C
(R6)3R:20981343G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20981343G>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20981343G>T
(R6)3R:20982042G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982042G>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982042G>T
(R6)3R:20978403C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20978403C>A
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20978403C>A
(R6)3R:20983781T>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20983781T>G
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20983781T>G
(R6)3R:20983963T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20983963T>A
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20983963T>A
(R6)3R:20982710G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982710G>A
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982710G>A
(R6)3R:20982763A>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982763A>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982763A>C
(R6)3R:20983466T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20983466T>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20983466T>C
CalxMB09693
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0219536
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
CalxMI04700
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0347815
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
CalxD
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0193747
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
CalxMB08599
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0218826
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3R:20980944_20980946delinsACA
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20980944_20980946delinsACA
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: MNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20980944_20980946delinsACA
(R6)3R:20981316G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20981316G>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20981316G>T
(R6)3R:20981392C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20981392C>A
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20981392C>A
(R6)3R:20981536G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20981536G>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20981536G>T
(R6)3R:20982105C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982105C>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982105C>T
(R6)3R:20982143G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982143G>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982143G>T
(R6)3R:20982271C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982271C>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982271C>T
(R6)3R:20982294C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982294C>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982294C>T
(R6)3R:20982506G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982506G>A
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982506G>A
(R6)3R:20989807T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20989807T>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20989807T>C
CalxJ033
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0388104
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
Calx0746-G4
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0320177
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3R:20978627G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20978627G>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20978627G>T
(R6)3R:20979001C>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20979001C>G
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20979001C>G
(R6)3R:20979655T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20979655T>A
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20979655T>A
(R6)3R:20979690T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20979690T>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20979690T>C
(R6)3R:20981366G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20981366G>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20981366G>T
(R6)3R:20981825C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20981825C>T
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20981825C>T
(R6)3R:20982102G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.20982102G>C
Genes: Calx (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:20982102G>C