Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CG6052 (Dme)
CG6052CR02725-TG4.2
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0388902
Genes: CG6052 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(R6)3L:17725848T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725848T>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725848T>A
(R6)3L:17725906G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725906G>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725906G>A
(R6)3L:17725912A>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725912A>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725912A>C
(R6)3L:17724522C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17724522C>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17724522C>T
(R6)3L:17727697T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727697T>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727697T>A
(R6)3L:17727871C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727871C>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727871C>A
(R6)3L:17726290G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726290G>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726290G>A
(R6)3L:17726905C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726905C>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726905C>A
(R6)3L:17727664T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727664T>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727664T>A
(R6)3L:17723809A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17723809A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17723809A>G
(R6)3L:17725588A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725588A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725588A>G
(R6)3L:17729299T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17729299T>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17729299T>C
(R6)3L:17726562A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726562A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726562A>G
(R6)3L:17726747C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726747C>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726747C>A
(R6)3L:17726896C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726896C>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726896C>T
(R6)3L:17727421A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727421A>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727421A>T
(R6)3L:17727559A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727559A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727559A>G
(R6)3L:17724099T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17724099T>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17724099T>C
(R6)3L:17724106G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17724106G>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17724106G>A
(R6)3L:17729081T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17729081T>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17729081T>C
(R6)3L:17726941C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726941C>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726941C>T
(R6)3L:17727002C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727002C>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727002C>A
(R6)3L:17727010T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727010T>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727010T>C
(R6)3L:17725213G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725213G>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725213G>T
(R6)3L:17726703C>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726703C>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726703C>G
(R6)3L:17729011T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17729011T>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17729011T>C
(R6)3L:17726584A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726584A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726584A>G
(R6)3L:17728465A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17728465A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17728465A>G
(R6)3L:17725606A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725606A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725606A>G
(R6)3L:17725657C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725657C>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725657C>T
CG6052MI03952
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0264487
Genes: CG6052 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3L:17725489T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725489T>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725489T>C
(R6)3L:17726266G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726266G>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726266G>C
(R6)3L:17723885A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17723885A>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17723885A>T
(R6)3L:17724161T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17724161T>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17724161T>C
(R6)3L:17724607A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17724607A>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17724607A>T
(R6)3L:17725447G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725447G>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725447G>T
(R6)3L:17726445T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17726445T>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17726445T>A
(R6)3L:17727165C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727165C>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727165C>T
(R6)3L:17727385G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727385G>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727385G>T
(R6)3L:17727859A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727859A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727859A>G
(R6)3L:17723993G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17723993G>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17723993G>A
(R6)3L:17727892G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727892G>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727892G>A
(R6)3L:17727976C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17727976C>T
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17727976C>T
(R6)3L:17725564A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725564A>G
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725564A>G
(R6)3L:17725087T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725087T>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725087T>A
(R6)3L:17725171T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17725171T>C
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17725171T>C
(R6)3L:17728402C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17728402C>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17728402C>A
(R6)3L:17728489G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.17728489G>A
Genes: CG6052 (Dme), Ccn (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:17728489G>A