Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CG10803 (Dme)
(R6)X:3489931G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3489931G>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3489931G>A
(R6)X:3490040T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3490040T>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3490040T>A
(R6)X:3488248C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3488248C>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3488248C>A
(R6)X:3487557A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487557A>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487557A>G
(R6)X:3489205C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3489205C>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3489205C>T
(R6)X:3489564A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3489564A>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3489564A>T
(R6)X:3486504A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486504A>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486504A>G
(R6)X:3486941G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486941G>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486941G>A
(R6)X:3487882A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487882A>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487882A>G
(R6)X:3486589A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486589A>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486589A>G
CG10803MI11338
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0297597
Genes: CG10803 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: non_coding_transcript_variant, coding_sequence_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:3487360T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487360T>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487360T>A
(R6)X:3486557G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486557G>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486557G>A
(R6)X:3486570T>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486570T>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486570T>G
(R6)X:3486725T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486725T>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486725T>A
(R6)X:3486864A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486864A>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486864A>G
(R6)X:3487352T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487352T>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487352T>C
(R6)X:3488156C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3488156C>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3488156C>T
(R6)X:3486333G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486333G>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486333G>T
(R6)X:3486371A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486371A>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486371A>T
(R6)X:3487767A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487767A>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487767A>T
CG10803EY04011
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0217125
Genes: CG10803 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
CG108030807-G4
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0317441
Genes: CG10803 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
CG10803MB09639
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0327106
Genes: CG10803 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:3486728T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486728T>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486728T>C
(R6)X:3487376C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487376C>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487376C>G
(R6)X:3486380T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486380T>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486380T>C
(R6)X:3487148C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487148C>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487148C>T
(R6)X:3487061G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487061G>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487061G>A
(R6)X:3487311T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487311T>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487311T>C
(R6)X:3485697C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3485697C>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3485697C>A
(R6)X:3486242C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486242C>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486242C>T
(R6)X:3487537G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487537G>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487537G>C
(R6)X:3489069A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3489069A>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3489069A>G
(R6)X:3488418T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3488418T>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3488418T>A
(R6)X:3490221A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3490221A>G
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3490221A>G
(R6)X:3487547C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487547C>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487547C>T
(R6)X:3487554C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487554C>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487554C>A
(R6)X:3488046T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3488046T>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3488046T>C
(R6)X:3485762G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3485762G>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3485762G>C
(R6)X:3486171G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486171G>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486171G>C
(R6)X:3486206C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486206C>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486206C>T
(R6)X:3490634C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3490634C>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3490634C>T
(R6)X:3488054G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3488054G>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3488054G>T
CG10803d02780
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0187788
Genes: CG10803 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:3487886C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487886C>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487886C>A
(R6)X:3487688G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487688G>C
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487688G>C
(R6)X:3486364C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486364C>T
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486364C>T
(R6)X:3486947C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3486947C>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3486947C>A
(R6)X:3487021C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.3487021C>A
Genes: lncRNA:CR44999 (Dme), CG10803 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3487021C>A