Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CG16952 (Dme)
CG16952GG01779
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0186957
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(R6)X:15871091C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15871091C>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15871091C>A
(R6)X:15872657A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872657A>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15872657A>C
(R6)X:15870325T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870325T>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870325T>C
(R6)X:15870330A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870330A>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870330A>C
(R6)X:15870667G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870667G>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870667G>T
(R6)X:15870802T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870802T>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870802T>C
(R6)X:15871642C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15871642C>G
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15871642C>G
(R6)X:15872677A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872677A>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15872677A>T
(R6)X:15875230C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15875230C>G
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15875230C>G
(R6)X:15870298T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870298T>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870298T>C
(R6)X:15872223T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872223T>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:15872223T>C
(R6)X:15873168G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15873168G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15873168G>A
(R6)X:15874581G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15874581G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15874581G>A
(R6)X:15870590_15870612delinsGTGGAGA
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870590_15870612delinsGTGGAGA
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870590_15870612delinsGTGGAGA
(R6)X:15870714G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870714G>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870714G>T
(R6)X:15870782A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870782A>G
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870782A>G
(R6)X:15873336A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15873336A>G
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15873336A>G
(R6)X:15874065T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15874065T>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15874065T>C
(R6)X:15871336T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15871336T>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15871336T>A
(R6)X:15871625T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15871625T>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15871625T>C
CG16952e03798
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0162087
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
CG16952e02352
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0222606
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:15875260C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15875260C>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:15875260C>T
(R6)X:15872452C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872452C>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15872452C>T
(R6)X:15874283A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15874283A>G
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:15874283A>G
(R6)X:15872760G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872760G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15872760G>A
(R6)X:15872485A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872485A>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15872485A>C
(R6)X:15874281A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15874281A>G
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15874281A>G
(R6)X:15870678C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870678C>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870678C>T
(R6)X:15872019C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872019C>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15872019C>T
(R6)X:15872646G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872646G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15872646G>A
(R6)X:15875239T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15875239T>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15875239T>A
(R6)X:15875250A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15875250A>C
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15875250A>C
(R6)X:15870618A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870618A>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870618A>T
(R6)X:15871378G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15871378G>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:15871378G>T
(R6)X:15872278G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872278G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15872278G>A
(R6)X:15873981G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15873981G>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15873981G>T
(R6)X:15872211G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872211G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:15872211G>A
(R6)X:15874722C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15874722C>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15874722C>T
(R6)X:15874824G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15874824G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15874824G>A
(R6)X:15870831C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870831C>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870831C>A
(R6)X:15872688C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872688C>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:15872688C>T
(R6)X:15870386G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15870386G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:15870386G>A
(R6)X:15871216T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15871216T>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:15871216T>A
(R6)X:15874950C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15874950C>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15874950C>T
(R6)X:15875323T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15875323T>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:15875323T>A
(R6)X:15874461G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15874461G>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15874461G>A
(R6)X:15872438C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15872438C>A
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15872438C>A
(R6)X:15873832C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.15873832C>T
Genes: CG16952 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:15873832C>T