Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CG18746 (Dme)
(R6)3R:7788546C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788546C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7788546C>T
(R6)3R:7788969A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788969A>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:7788969A>T
(R6)3R:7790171C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7790171C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3R:7790171C>T
(R6)3R:7788548G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788548G>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:7788548G>C
(R6)3R:7789772A>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789772A>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7789772A>C
(R6)3R:7788282G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788282G>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3R:7788282G>C
(R6)3R:7789237T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789237T>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7789237T>C
(R6)3R:7789715T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789715T>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7789715T>A
(R6)3R:7789943C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789943C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7789943C>T
(R6)3R:7789898G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789898G>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7789898G>A
(R6)3R:7788949G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788949G>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7788949G>C
(R6)3R:7789621C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789621C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7789621C>T
(R6)3R:7788369C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788369C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3R:7788369C>T
(R6)3R:7788675G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788675G>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7788675G>A
(R6)3R:7789963T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789963T>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7789963T>C
(R6)3R:7788486T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788486T>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_retained_variant
Diseases: Not Available
Variant Name: (R6)3R:7788486T>C
(R6)3R:7788837T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788837T>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:7788837T>C
(R6)3R:7789221T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789221T>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:7789221T>C
(R6)3R:7789597A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789597A>G
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7789597A>G
(R6)3R:7789735G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789735G>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7789735G>A
(R6)3R:7789039C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789039C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (R6)3R:7789039C>T
(R6)3R:7788597T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788597T>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7788597T>C
(R6)3R:7789264G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789264G>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7789264G>T
(R6)3R:7788761C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788761C>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (R6)3R:7788761C>A
(R6)3R:7788422T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788422T>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:7788422T>C
(R6)3R:7788415C>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788415C>G
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7788415C>G
(R6)3R:7788835C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788835C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7788835C>T
(R6)3R:7789413G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789413G>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7789413G>A
(R6)3R:7789572G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789572G>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:7789572G>A
(R6)3R:7788730A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788730A>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7788730A>T
(R6)3R:7789808G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789808G>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7789808G>C
(R6)3R:7788636G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788636G>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7788636G>A
(R6)3R:7790126T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7790126T>C
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3R:7790126T>C
(R6)3R:7789368A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789368A>G
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7789368A>G
(R6)3R:7788353C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788353C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3R:7788353C>T
(R6)3R:7789382C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789382C>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7789382C>T
(R6)3R:7788540T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7788540T>A
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:7788540T>A
(R6)3R:7789930A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.7789930A>T
Genes: CG18746 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:7789930A>T