Version: 8.0.0
Date: Tue Jan 28 2025
465 results
Allele/Variant Genes: CG11658 (Dme)

CG11658GS22038

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0360016
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: attention deficit hyperactivity disorder
Variant Name: Not Available

CG11658EY10315

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0162541
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: attention deficit hyperactivity disorder
Variant Name: Not Available

(R6)3L:11700595C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11700595C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3L:11700595C>T

(R6)3L:11702335G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11702335G>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11702335G>A

(R6)3L:11703678C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11703678C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11703678C>T

(R6)3L:11703956C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11703956C>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11703956C>A

(R6)3L:11704642G>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11704642G>C
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11704642G>C

(R6)3L:11704716T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11704716T>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11704716T>A

(R6)3L:11704722C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11704722C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11704722C>T

(R6)3L:11704751G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11704751G>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11704751G>A

(R6)3L:11704759C>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11704759C>G
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11704759C>G

(R6)3L:11704810G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11704810G>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11704810G>A

CG11658KG07792

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0318953
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available

CG11658KG08620

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0223977
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

CG11658EP3534

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0223975
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(R6)3L:11699687A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11699687A>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3L:11699687A>T

(R6)3L:11702290G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11702290G>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11702290G>T

(R6)3L:11702375G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11702375G>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11702375G>A

(R6)3L:11702426T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11702426T>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11702426T>A

(R6)3L:11703316C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11703316C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11703316C>T

(R6)3L:11703369A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11703369A>G
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11703369A>G

(R6)3L:11703470_11703472delinsACAACA

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11703470_11703472delinsACAACA
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11703470_11703472delinsACAACA

(R6)3L:11703481T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11703481T>C
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11703481T>C

(R6)3L:11706999T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11706999T>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11706999T>A

(R6)3L:11707510T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11707510T>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3L:11707510T>A

CG116580493-G4

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0317450
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(R6)3L:11701379C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11701379C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3L:11701379C>T

(R6)3L:11701440A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11701440A>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11701440A>T

(R6)3L:11701817C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11701817C>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11701817C>A

(R6)3L:11705514C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11705514C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11705514C>T

(R6)3L:11705549G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11705549G>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11705549G>T

(R6)3L:11705568T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11705568T>C
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11705568T>C

(R6)3L:11705691C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11705691C>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11705691C>A

(R6)3L:11706170C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11706170C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11706170C>T

(R6)3L:11705893G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11705893G>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11705893G>A

(R6)3L:11705972T>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11705972T>G
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11705972T>G

CG11658MI03370

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0267448
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

CG116585-HA-2091

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0223976
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available

CG11658c05508

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0187609
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

CG11658MI03370-TG4.2

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0323725
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(R6)3L:11707655G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11707655G>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11707655G>A

(R6)3L:11707829C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11707829C>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11707829C>A

(R6)3L:11707052A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11707052A>G
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11707052A>G

(R6)3L:11708049A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11708049A>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11708049A>T

(R6)3L:11708271G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11708271G>A
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11708271G>A

(R6)3L:11703569A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11703569A>G
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11703569A>G

(R6)3L:11704234C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11704234C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11704234C>T

(R6)3L:11701806C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11701806C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11701806C>T

(R6)3L:11700183C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11700183C>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3L:11700183C>T

(R6)3L:11705895G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_037436.4:g.11705895G>T
Genes: CG11658 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:11705895G>T