Version: 8.0.0
Date: Tue Jan 28 2025
64 results
Allele/Variant Genes: Sap30 (Dme)

Sap30CR02936-TG4.0

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0388980
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

(R6)X:16787691G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787691G>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787691G>A

(R6)X:16787752T>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787752T>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787752T>G

(R6)X:16788388C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788388C>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16788388C>T

(R6)X:16788496delinsCA

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788496delinsCA
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16788496delinsCA

(R6)X:16788527T>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788527T>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16788527T>G

(R6)X:16788866G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788866G>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16788866G>T

(R6)X:16787478A>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787478A>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787478A>T

(R6)X:16787669G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787669G>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16787669G>T

(R6)X:16789209C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789209C>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789209C>A

(R6)X:16788394C>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788394C>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16788394C>G

(R6)X:16789361A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789361A>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789361A>G

(R6)X:16789379T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789379T>C
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789379T>C

(R6)X:16788276G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788276G>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16788276G>A

(R6)X:16788498C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788498C>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16788498C>A

(R6)X:16787452C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787452C>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787452C>T

(R6)X:16787690T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787690T>C
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787690T>C

(R6)X:16787628A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787628A>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16787628A>G

(R6)X:16788368G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788368G>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16788368G>A

(R6)X:16787697C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787697C>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787697C>A

(R6)X:16787717T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787717T>C
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787717T>C

Sap30G17819

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0248652
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available

(R6)X:16787726G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787726G>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787726G>A

(R6)X:16787359A>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787359A>C
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787359A>C

(R6)X:16787322T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787322T>C
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787322T>C

(R6)X:16787427G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787427G>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787427G>T

(R6)X:16787480T>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787480T>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787480T>G

(R6)X:16787653T>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787653T>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16787653T>A

(R6)X:16789583A>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789583A>C
Genes: Sap30 (Dme), Rrp45 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789583A>C

(R6)X:16787406G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787406G>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787406G>A

(R6)X:16787516G>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787516G>C
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787516G>C

(R6)X:16787638A>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787638A>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16787638A>T

(R6)X:16787747C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787747C>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787747C>T

(R6)X:16789398C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789398C>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789398C>T

(R6)X:16789556C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789556C>A
Genes: Sap30 (Dme), Rrp45 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789556C>A

(R6)X:16787485T>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787485T>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787485T>G

(R6)X:16787703A>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787703A>C
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787703A>C

(R6)X:16789049A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789049A>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789049A>G

(R6)X:16787852C>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787852C>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787852C>G

(R6)X:16788099G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788099G>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:16788099G>A

(R6)X:16788402C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788402C>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16788402C>T

(R6)X:16787306A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787306A>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787306A>G

(R6)X:16788788C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16788788C>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16788788C>A

(R6)X:16789111G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789111G>T
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789111G>T

(R6)X:16789362A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789362A>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789362A>G

(R6)X:16789493G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789493G>T
Genes: Sap30 (Dme), Rrp45 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789493G>T

(R6)X:16789387C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16789387C>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16789387C>A

(R6)X:16787397A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787397A>G
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787397A>G

(R6)X:16787746C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787746C>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:16787746C>A

(R6)X:16787645T>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.16787645T>A
Genes: Sap30 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:16787645T>A