Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CG1622 (Dme) Molecular Consequence: missense variant
(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:13299398A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.13299398A>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:13299398A>G
(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