Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: nod (Dme)
nodunspecified
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0051326
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
nodf04008
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0158884
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
nod2
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013066
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
nod6
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013070
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
nod9
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0035281
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
nod3
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013067
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
nodDR1
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0035282
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
nodDR4
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013075
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
nod5
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013069
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
nod1
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013065
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(R6)X:11584750G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584750G>A
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11584750G>A
(R6)X:11585380C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585380C>G
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11585380C>G
(R6)X:11584260G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584260G>C
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:11584260G>C
(R6)X:11584720C>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584720C>A
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11584720C>A
(R6)X:11583411A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11583411A>C
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:11583411A>C
(R6)X:11582265C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11582265C>T
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:11582265C>T
(R6)X:11584622A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584622A>G
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11584622A>G
(R6)X:11582156T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11582156T>A
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:11582156T>A
nodA4579T
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0098677
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
nodDTW
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013072
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
nodDR2
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013074
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
nodf01431
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178655
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: coding_sequence_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:11581437G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11581437G>T
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11581437G>T
(R6)X:11584016T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584016T>C
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:11584016T>C
(R6)X:11583699T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11583699T>A
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:11583699T>A
(R6)X:11585098C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585098C>T
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11585098C>T
(R6)X:11585377T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585377T>A
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11585377T>A
(R6)X:11583736T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11583736T>C
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:11583736T>C
(R6)X:11585368G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585368G>A
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11585368G>A
(R6)X:11585749A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585749A>T
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:11585749A>T
(R6)X:11584452T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584452T>C
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:11584452T>C
(R6)X:11585300T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585300T>C
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:11585300T>C
nod143
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0284466
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
nodEY01772
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0158885
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
nod4
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013068
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant, stop_lost, start_lost, splice_donor_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
nodDR3
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013073
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
(R6)X:11584834A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584834A>C
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11584834A>C
(R6)X:11584229T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584229T>C
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:11584229T>C
(R6)X:11585432A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585432A>T
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11585432A>T
(R6)X:11585735T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585735T>A
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:11585735T>A
(R6)X:11582923G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11582923G>A
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:11582923G>A
(R6)X:11584150G>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584150G>C
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:11584150G>C
(R6)X:11584584G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584584G>A
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:11584584G>A
(R6)X:11585304T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11585304T>C
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:11585304T>C
(R6)X:11583581G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11583581G>A
Genes: nod (Dme), pkm (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:11583581G>A
(R6)X:11581059G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11581059G>T
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:11581059G>T
node03334
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0178656
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: coding_sequence_variant
Diseases: Not Available
Variant Name: Not Available
noda
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0013064
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
(R6)X:11584994C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11584994C>G
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:11584994C>G
(R6)X:11581852G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.11581852G>T
Genes: nod (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:11581852G>T