Version: 8.0.0
Date: Tue Jan 28 2025
13 results
Allele/Variant Genes: CG2063 (Dme)

(R6)2R:9286064G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286064G>A
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2R:9286064G>A

(R6)2R:9286466G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286466G>A
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2R:9286466G>A

CG2063MI05311

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0280634
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available

(R6)2R:9286248C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286248C>T
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2R:9286248C>T

(R6)2R:9286398T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286398T>C
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2R:9286398T>C

(R6)2R:9286259G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286259G>T
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2R:9286259G>T

(R6)2R:9286287C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286287C>T
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2R:9286287C>T

(R6)2R:9286297C>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286297C>G
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2R:9286297C>G

CG2063f04520

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0186671
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available

(R6)2R:9285579A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9285579A>G
Genes: asRNA:CR45132 (Dme), CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)2R:9285579A>G

(R6)2R:9286622T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286622T>A
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2R:9286622T>A

(R6)2R:9286039G>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286039G>C
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2R:9286039G>C

(R6)2R:9286442C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033778.4:g.9286442C>T
Genes: CG2063 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2R:9286442C>T