Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: nudC (Dme)
nudC9jE8
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0221535
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(R6)3L:16808324G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16808324G>A
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16808324G>A
(R6)3L:16808690C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16808690C>T
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16808690C>T
(R6)3L:16809754G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16809754G>A
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16809754G>A
(R6)3L:16812045G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16812045G>A
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16812045G>A
(R6)3L:16812058T>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16812058T>G
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16812058T>G
(R6)3L:16807158T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16807158T>C
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16807158T>C
(R6)3L:16807566A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16807566A>G
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16807566A>G
(R6)3L:16814340C>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16814340C>G
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16814340C>G
(R6)3L:16814405G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16814405G>A
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16814405G>A
(R6)3L:16808995T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16808995T>C
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16808995T>C
nudCCPTI003161
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0261661
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
nudCf05219
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178623
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3L:16805862T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16805862T>C
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16805862T>C
(R6)3L:16805907C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16805907C>A
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16805907C>A
(R6)3L:16806136G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806136G>C
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806136G>C
(R6)3L:16805283G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16805283G>T
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16805283G>T
(R6)3L:16808610C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16808610C>T
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3L:16808610C>T
(R6)3L:16812538T>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16812538T>G
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16812538T>G
(R6)3L:16812791C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16812791C>T
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16812791C>T
(R6)3L:16813124G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16813124G>A
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16813124G>A
(R6)3L:16807279A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16807279A>G
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16807279A>G
(R6)3L:16814097C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16814097C>T
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16814097C>T
nudCG11883
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0372963
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
nudCG19348
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0372965
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
nudCMI04357
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0352856
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
nudCc04337
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178624
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3L:16805552A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16805552A>T
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16805552A>T
(R6)3L:16806051C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806051C>T
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806051C>T
(R6)3L:16806195T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806195T>C
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806195T>C
(R6)3L:16806944T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806944T>C
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806944T>C
(R6)3L:16805115C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16805115C>T
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16805115C>T
(R6)3L:16809549C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16809549C>T
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16809549C>T
(R6)3L:16809552T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16809552T>C
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16809552T>C
(R6)3L:16811903G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16811903G>A
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16811903G>A
(R6)3L:16812973C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16812973C>A
Genes: nudC (Dme), CG13024 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16812973C>A
(R6)3L:16809030A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16809030A>T
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16809030A>T
nudCG4826
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0372966
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
nudCG15713
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0372964
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
nudCNP0672
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0357966
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
nudC2114-G4
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0320316
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
nudCPL00045
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0158877
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
nudCc04336
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178625
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
nudCc03957
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178626
Genes: nudC (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3L:16805784A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16805784A>T
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16805784A>T
(R6)3L:16806144A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806144A>G
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806144A>G
(R6)3L:16806276T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806276T>C
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806276T>C
(R6)3L:16806380A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806380A>T
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806380A>T
(R6)3L:16806648C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806648C>A
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806648C>A
(R6)3L:16806951G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.16806951G>C
Genes: nudC (Dme), CG9674 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3L:16806951G>C