Version: 8.0.0
Date: Tue Jan 28 2025
86 results
Allele/Variant Genes: CG15406 (Dme)

(R6)2L:3310966G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310966G>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310966G>A

(R6)2L:3310933A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310933A>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310933A>G

(R6)2L:3311033C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311033C>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311033C>A

(R6)2L:3309988C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309988C>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309988C>T

(R6)2L:3310181C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310181C>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310181C>T

(R6)2L:3309328C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309328C>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309328C>A

(R6)2L:3309330C>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309330C>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309330C>G

(R6)2L:3310457T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310457T>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310457T>A

(R6)2L:3311372A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311372A>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311372A>G

(R6)2L:3311540T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311540T>C
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311540T>C

(R6)2L:3310382T>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310382T>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310382T>G

(R6)2L:3310393C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310393C>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310393C>T

(R6)2L:3310479G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310479G>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310479G>A

(R6)2L:3310834A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310834A>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310834A>G

(R6)2L:3311002G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311002G>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311002G>A

(R6)2L:3311525T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311525T>C
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311525T>C

(R6)2L:3309946T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309946T>C
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309946T>C

(R6)2L:3311240G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311240G>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311240G>A

(R6)2L:3310336C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310336C>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310336C>A

(R6)2L:3310524T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310524T>C
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310524T>C

CG15406SK1

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0381586
Genes: CG15406 (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available

CG15406f05661

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0162169
Genes: CG15406 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(R6)2L:3309362G>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309362G>C
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309362G>C

(R6)2L:3309369G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309369G>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309369G>A

(R6)2L:3310058C>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310058C>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310058C>G

(R6)2L:3310306T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310306T>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310306T>A

(R6)2L:3310339_3310341delinsTGT

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310339_3310341delinsTGT
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: MNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310339_3310341delinsTGT

(R6)2L:3309976G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309976G>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309976G>A

(R6)2L:3310031T>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310031T>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310031T>G

(R6)2L:3309359G>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309359G>C
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309359G>C

(R6)2L:3310313T>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310313T>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310313T>G

(R6)2L:3310458A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310458A>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310458A>T

CG15406SK3

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0381587
Genes: CG15406 (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available

(R6)2L:3310094T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310094T>C
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310094T>C

(R6)2L:3310939C>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310939C>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310939C>G

(R6)2L:3309320T>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309320T>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309320T>G

(R6)2L:3309418A>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309418A>C
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309418A>C

(R6)2L:3309518T>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309518T>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309518T>G

(R6)2L:3309596C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309596C>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309596C>T

(R6)2L:3311189A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311189A>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311189A>T

(R6)2L:3310250T>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310250T>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310250T>G

(R6)2L:3311156G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311156G>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311156G>A

(R6)2L:3311363C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3311363C>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3311363C>A

(R6)2L:3310059C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310059C>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310059C>T

(R6)2L:3309422C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309422C>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309422C>A

(R6)2L:3309552T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309552T>A
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309552T>A

(R6)2L:3309687G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309687G>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309687G>T

(R6)2L:3309983G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309983G>T
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309983G>T

(R6)2L:3309844A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3309844A>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3309844A>G

(R6)2L:3310470A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.3310470A>G
Genes: CG3277 (Dme), CG15406 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:3310470A>G