Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CG1622 (Dme)
(R6)X:13297133A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297133A>G
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297133A>G
(R6)X:13297779A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297779A>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297779A>C
(R6)X:13298866G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298866G>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298866G>T
(R6)X:13297725T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297725T>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297725T>C
(R6)X:13299267C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299267C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299267C>T
(R6)X:13297954C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297954C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297954C>T
(R6)X:13298976G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298976G>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298976G>T
(R6)X:13299306G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299306G>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299306G>T
(R6)X:13299315A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299315A>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299315A>C
(R6)X:13298658T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298658T>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298658T>A
(R6)X:13298025T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298025T>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298025T>A
(R6)X:13298666G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298666G>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298666G>T
(R6)X:13298077C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298077C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298077C>T
(R6)X:13297716C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297716C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297716C>T
(R6)X:13297990T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297990T>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297990T>A
(R6)X:13299360T>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299360T>G
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299360T>G
(R6)X:13297389C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297389C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297389C>T
(R6)X:13297399C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297399C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297399C>T
(R6)X:13298404delinsTC
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298404delinsTC
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298404delinsTC
(R6)X:13299288T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299288T>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299288T>C
(R6)X:13298071G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298071G>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298071G>A
(R6)X:13297736T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297736T>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297736T>A
(R6)X:13297743C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297743C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297743C>T
(R6)X:13298395C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298395C>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298395C>A
(R6)X:13297460C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297460C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297460C>T
(R6)X:13298544delinsTAA
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298544delinsTAA
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298544delinsTAA
(R6)X:13299330C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299330C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299330C>T
(R6)X:13299353A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299353A>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299353A>C
(R6)X:13299540A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299540A>G
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299540A>G
(R6)X:13299648T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299648T>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299648T>C
(R6)X:13299498C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299498C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299498C>T
(R6)X:13297821G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297821G>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297821G>A
(R6)X:13298419C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298419C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298419C>T
(R6)X:13298535T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298535T>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298535T>A
(R6)X:13297211T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297211T>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297211T>C
(R6)X:13297985C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297985C>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297985C>A
(R6)X:13298053C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298053C>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298053C>A
(R6)X:13298595A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298595A>G
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298595A>G
(R6)X:13298689T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298689T>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298689T>C
(R6)X:13298127A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298127A>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298127A>T
(R6)X:13298973C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298973C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298973C>T
(R6)X:13298029T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298029T>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298029T>C
(R6)X:13298484A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298484A>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298484A>C
(R6)X:13298519A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298519A>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298519A>T
(R6)X:13297969C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13297969C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13297969C>T
(R6)X:13298008G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298008G>C
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298008G>C
(R6)X:13298084G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298084G>A
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298084G>A
(R6)X:13298636C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298636C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298636C>T
(R6)X:13299609C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299609C>T
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13299609C>T
(R6)X:13298157A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13298157A>G
Genes: CG1622 (Dme), CG1764 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:13298157A>G