Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Diseases
Genes
Allele/Variant Genes: htt (Dme)
htt98E2
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0241668
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Huntington's disease
Variant Name: Not Available
httKO
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0328074
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Huntington's disease
Variant Name: Not Available
httint
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0324927
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
httΔ
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0324928
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
httCR70494-TG4.2
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0386754
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(R6)3R:28696456G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28696456G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28696456G>A
(R6)3R:28696608G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28696608G>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28696608G>T
(R6)3R:28696639T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28696639T>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28696639T>A
(R6)3R:28705288A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28705288A>G
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28705288A>G
(R6)3R:28707355A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28707355A>G
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28707355A>G
(R6)3R:28708117A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28708117A>G
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28708117A>G
(R6)3R:28699612G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28699612G>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28699612G>T
(R6)3R:28700467A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28700467A>G
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:28700467A>G
(R6)3R:28710363C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28710363C>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:28710363C>T
(R6)3R:28705869T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28705869T>C
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28705869T>C
httMB03997
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0198253
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3R:28702197A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28702197A>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28702197A>T
(R6)3R:28704312G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28704312G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28704312G>A
(R6)3R:28704849T>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28704849T>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28704849T>A
(R6)3R:28704984C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28704984C>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28704984C>T
(R6)3R:28705034G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28705034G>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28705034G>T
(R6)3R:28696937G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28696937G>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28696937G>T
(R6)3R:28708131G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28708131G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28708131G>A
(R6)3R:28708154G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28708154G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28708154G>A
(R6)3R:28706621G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28706621G>C
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:28706621G>C
(R6)3R:28708798G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28708798G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:28708798G>A
httMI01636
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0260295
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
httMI04607
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0267263
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
httc05407
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0179429
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
httf05417
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0179427
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3R:28719139G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28719139G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28719139G>A
(R6)3R:28719268T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28719268T>C
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28719268T>C
(R6)3R:28719269C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28719269C>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28719269C>T
(R6)3R:28717614G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28717614G>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28717614G>T
(R6)3R:28717745C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28717745C>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28717745C>A
(R6)3R:28717905A>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28717905A>C
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28717905A>C
(R6)3R:28717945A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28717945A>G
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28717945A>G
(R6)3R:28718063A>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28718063A>C
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28718063A>C
(R6)3R:28718068G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28718068G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28718068G>A
(R6)3R:28718425T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28718425T>C
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28718425T>C
httf04684
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0179428
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
httMI04607-GFSTF.1
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0314539
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(R6)3R:28696515C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28696515C>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28696515C>A
(R6)3R:28697418G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28697418G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28697418G>A
(R6)3R:28702202G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28702202G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28702202G>A
(R6)3R:28702215G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28702215G>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28702215G>T
(R6)3R:28704221A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28704221A>G
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28704221A>G
(R6)3R:28704608G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28704608G>A
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28704608G>A
(R6)3R:28704995G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28704995G>C
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)3R:28704995G>C
(R6)3R:28697094C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033777.3:g.28697094C>T
Genes: htt (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:28697094C>T