Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CG3632 (Dme)
CG3632KO
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0371109
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
CG3632m1
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0364795
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(R6)X:16299732G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16299732G>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16299732G>T
(R6)X:16303201A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16303201A>G
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16303201A>G
(R6)X:16300914A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16300914A>C
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16300914A>C
(R6)X:16302857C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16302857C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16302857C>T
(R6)X:16302185G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16302185G>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16302185G>A
(R6)X:16302793C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16302793C>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16302793C>A
(R6)X:16302903T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16302903T>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16302903T>A
(R6)X:16302803G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16302803G>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16302803G>A
(R6)X:16297536G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297536G>A
Genes: ERp44 (Dme), CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297536G>A
(R6)X:16297841A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297841A>C
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297841A>C
CG3632EY11966
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0161480
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: coding_sequence_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:16302798G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16302798G>C
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16302798G>C
(R6)X:16298326C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298326C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:16298326C>T
(R6)X:16300042A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16300042A>G
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16300042A>G
(R6)X:16300120A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16300120A>G
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16300120A>G
(R6)X:16298879G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298879G>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16298879G>A
(R6)X:16297249T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297249T>C
Genes: ERp44 (Dme), CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297249T>C
(R6)X:16297953T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297953T>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:16297953T>A
(R6)X:16298327C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298327C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16298327C>T
(R6)X:16297895C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297895C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16297895C>T
(R6)X:16298471C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298471C>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16298471C>A
(R6)X:16302730C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16302730C>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16302730C>A
(R6)X:16297247C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297247C>G
Genes: ERp44 (Dme), CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297247C>G
(R6)X:16299736G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16299736G>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16299736G>T
(R6)X:16303132C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16303132C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16303132C>T
(R6)X:16297846T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297846T>C
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297846T>C
(R6)X:16298861G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298861G>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16298861G>T
(R6)X:16298884T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298884T>C
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16298884T>C
(R6)X:16300713A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16300713A>G
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16300713A>G
(R6)X:16301540T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16301540T>C
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16301540T>C
(R6)X:16299614C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16299614C>G
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16299614C>G
(R6)X:16303097G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16303097G>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16303097G>A
(R6)X:16297000G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297000G>A
Genes: ERp44 (Dme), CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297000G>A
(R6)X:16297792T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297792T>C
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297792T>C
(R6)X:16298845G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298845G>C
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16298845G>C
(R6)X:16298893C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298893C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16298893C>T
(R6)X:16298985T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298985T>A
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16298985T>A
(R6)X:16303254A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16303254A>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16303254A>T
(R6)X:16301803A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16301803A>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16301803A>T
(R6)X:16298996delinsTAAAATCTTAAAATCAA
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16298996delinsTAAAATCTTAAAATCAA
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16298996delinsTAAAATCTTAAAATCAA
(R6)X:16297110G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297110G>T
Genes: ERp44 (Dme), CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297110G>T
CG3632MB03514
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0197001
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
CG3632e04331
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0161479
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: coding_sequence_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:16299783C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16299783C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16299783C>T
(R6)X:16297424C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16297424C>T
Genes: ERp44 (Dme), CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16297424C>T
(R6)X:16300206C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16300206C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16300206C>T
(R6)X:16301550G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16301550G>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16301550G>T
(R6)X:16301153C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.16301153C>T
Genes: CG3632 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16301153C>T