Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Genes
Allele/Variant Genes: scu (Dme)
scuunspecified
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0387007
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
scuPG115
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0129092
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(R6)X:18091412A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091412A>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091412A>G
(R6)X:18091862G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091862G>T
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091862G>T
(R6)X:18091831G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091831G>A
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091831G>A
(R6)X:18091873G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091873G>C
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091873G>C
(R6)X:18092254C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18092254C>T
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:18092254C>T
(R6)X:18092837A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18092837A>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:18092837A>G
scu174
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0006237
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
scuKO7
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0368907
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available
scuS152
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0090140
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
scuA
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0291330
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
scuB
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0324299
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
scu4058
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0034857
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:18091309C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091309C>T
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:18091309C>T
(R6)X:18091868G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091868G>A
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091868G>A
(R6)X:18091318C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091318C>T
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:18091318C>T
(R6)X:18091446G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091446G>A
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091446G>A
(R6)X:18091606T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091606T>C
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091606T>C
(R6)X:18091816T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091816T>A
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091816T>A
(R6)X:18091923T>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091923T>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091923T>G
(R6)X:18091948C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091948C>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091948C>G
(R6)X:18092632G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18092632G>A
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:18092632G>A
(R6)X:18091577A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091577A>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091577A>G
(R6)X:18091730T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091730T>A
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091730T>A
(R6)X:18091907T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091907T>A
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091907T>A
(R6)X:18091870A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091870A>T
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091870A>T
scuD
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0291331
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
scuf05779
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178086
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
scu3127
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0090141
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available
scuf05851
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0158692
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:18091394C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091394C>T
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091394C>T
(R6)X:18091511T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091511T>C
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091511T>C
(R6)X:18091425G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091425G>A
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091425G>A
(R6)X:18091501C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091501C>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091501C>G
(R6)X:18091808A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091808A>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091808A>G
(R6)X:18091456C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091456C>T
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091456C>T
(R6)X:18091931C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18091931C>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:18091931C>G
(R6)X:18092723A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.18092723A>G
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:18092723A>G
scue00459
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0222578
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
scuKO11
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0368908
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available
scue04520
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178088
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
scuf05767
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178087
Genes: scu (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available