122 results
Allele/Variant Genes: Pde4 (Dme) Molecular Consequence: synonymous variant

(R6)X:3241887A>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3241887A>C
Genes: Pde4 (Dme), ng3 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3241887A>C

(R6)X:3250536C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3250536C>A
Genes: Pde4 (Dme), Sgs4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3250536C>A

(R6)X:3250557C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3250557C>A
Genes: Pde4 (Dme), Sgs4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3250557C>A

(R6)X:3280538A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3280538A>G
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3280538A>G

(R6)X:3315303C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315303C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315303C>T

(R6)X:3315324G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315324G>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315324G>T

(R6)X:3314339C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314339C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314339C>T

(R6)X:3314430C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314430C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314430C>T

(R6)X:3316008A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3316008A>G
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3316008A>G

(R6)X:3280733A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3280733A>G
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3280733A>G

(R6)X:3281111A>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3281111A>C
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3281111A>C

(R6)X:3329713C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3329713C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3329713C>T

(R6)X:3314535A>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314535A>C
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314535A>C

(R6)X:3337288T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3337288T>C
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3337288T>C

(R6)X:3315996G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315996G>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315996G>A

(R6)X:3334202C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3334202C>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3334202C>A

(R6)X:3280190G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3280190G>A
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3280190G>A

(R6)X:3280886G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3280886G>T
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3280886G>T

(R6)X:3316239A>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3316239A>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3316239A>T

(R6)X:3315315G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315315G>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315315G>A

(R6)X:3314399T>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314399T>G
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314399T>G

(R6)X:3339050A>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3339050A>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3339050A>T

(R6)X:3314949C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314949C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314949C>T

(R6)X:3280211C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3280211C>A
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3280211C>A

(R6)X:3314850G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314850G>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314850G>A

(R6)X:3313934C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3313934C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3313934C>T

(R6)X:3337537C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3337537C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3337537C>T

(R6)X:3315948C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315948C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315948C>T

(R6)X:3315555C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315555C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315555C>T

(R6)X:3315852G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315852G>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315852G>A

(R6)X:3334214A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3334214A>G
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3334214A>G

(R6)X:3316058G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3316058G>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3316058G>A

(R6)X:3315684T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315684T>C
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315684T>C

(R6)X:3314940A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314940A>G
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314940A>G

(R6)X:3241815A>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3241815A>C
Genes: Pde4 (Dme), ng3 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3241815A>C

(R6)X:3244051G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3244051G>A
Genes: Pde4 (Dme), ng4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3244051G>A

(R6)X:3246434G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3246434G>A
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:3246434G>A

(R6)X:3245996T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3245996T>C
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:3245996T>C

(R6)X:3281084C>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3281084C>G
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3281084C>G

(R6)X:3315144T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315144T>C
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315144T>C

(R6)X:3339071T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3339071T>C
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3339071T>C

(R6)X:3280313C>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3280313C>G
Genes: Pde4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3280313C>G

(R6)X:3313802G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3313802G>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3313802G>A

(R6)X:3313931T>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3313931T>G
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3313931T>G

(R6)X:3315366G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315366G>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315366G>A

(R6)X:3314195G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314195G>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314195G>A

(R6)X:3315924C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3315924C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme), CG10793 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3315924C>T

(R6)X:3338801C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3338801C>T
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3338801C>T

(R6)X:3314001C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3314001C>A
Genes: Pde4 (Dme), lncRNA:CR44886 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3314001C>A

(R6)X:3250128G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.3250128G>A
Genes: Pde4 (Dme), Sgs4 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:3250128G>A