Version: 8.0.0
Date: Tue Jan 28 2025
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All
All
Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Allele/Variant
Show all Categories
Species
Drosophila melanogaster
239
×
Category
variant
233
×
allele
3
×
allele with one variant
3
×
Variant Type
SNP
231
×
unreported
3
×
delins
2
×
insertion
2
×
deletion
1
×
Molecular Consequence
intron variant
233
×
5 prime UTR variant
13
×
3 prime UTR variant
7
×
synonymous variant
5
×
missense variant
3
×
Genes
Timp (Dme)
239
×
Syn (Dme)
233
×
Filter
239
results
Page 1 of 5
Allele/Variant
Genes: Timp (Dme)
Timp
P1+P2
(
Drosophila melanogaster
)
Allele/Variant
Source:
FB:FBal0218944
Genes:
Timp (Dme)
Synonyms:
Not Available
Variant Type:
unreported
Molecular Consequence:
Not Available
Diseases:
Not Available
Variant Name:
Not Available
Gene (1)
Timp
28
(
Drosophila melanogaster
)
Allele/Variant
Source:
FB:FBal0218943
Genes:
Timp (Dme)
Synonyms:
Not Available
Variant Type:
unreported
Molecular Consequence:
Not Available
Diseases:
Not Available
Variant Name:
Not Available
Gene (1)
Timp
GFP
(
Drosophila melanogaster
)
Allele/Variant
Source:
FB:FBal0359912
Genes:
Timp (Dme)
Synonyms:
Not Available
Variant Type:
unreported
Molecular Consequence:
Not Available
Diseases:
Not Available
Variant Name:
Not Available
Gene (1)
(R6)3R:10205645C>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10205645C>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10205645C>T
(R6)3R:10208176C>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208176C>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208176C>T
(R6)3R:10208180A>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208180A>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208180A>G
(R6)3R:10211774T>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10211774T>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10211774T>C
(R6)3R:10208345T>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208345T>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208345T>G
(R6)3R:10212259T>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10212259T>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10212259T>A
(R6)3R:10208385C>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208385C>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208385C>T
(R6)3R:10209006G>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10209006G>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10209006G>C
(R6)3R:10209065G>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10209065G>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10209065G>A
(R6)3R:10209603T>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10209603T>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10209603T>A
Timp
S1
(
Drosophila melanogaster
)
Allele/Variant
Source:
FB:FBal0340174
Genes:
Timp (Dme)
Synonyms:
Not Available
Variant Type:
deletion
Molecular Consequence:
5_prime_UTR_variant, intron_variant
Diseases:
Not Available
Variant Name:
Not Available
Timp
MB01857
(
Drosophila melanogaster
)
Allele/Variant
Source:
FB:FBal0192211
Genes:
Timp (Dme)
Synonyms:
Not Available
Variant Type:
insertion
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
Not Available
(R6)3R:10207410G>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10207410G>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10207410G>A
(R6)3R:10206249C>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10206249C>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10206249C>G
(R6)3R:10206475G>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10206475G>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10206475G>A
(R6)3R:10207535A>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10207535A>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10207535A>G
(R6)3R:10207543G>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10207543G>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10207543G>C
(R6)3R:10207668T>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10207668T>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10207668T>A
(R6)3R:10209894A>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10209894A>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10209894A>G
(R6)3R:10212566T>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10212566T>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10212566T>A
(R6)3R:10205443C>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10205443C>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
5_prime_UTR_variant, intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10205443C>T
(R6)3R:10208133A>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208133A>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208133A>T
Timp
MI11389
(
Drosophila melanogaster
)
Allele/Variant
Source:
FB:FBal0297615
Genes:
Timp (Dme)
Synonyms:
Not Available
Variant Type:
insertion
Molecular Consequence:
5_prime_UTR_variant, intron_variant
Diseases:
Not Available
Variant Name:
Not Available
(R6)3R:10204970G>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10204970G>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant, intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10204970G>T
(R6)3R:10205257C>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10205257C>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
5_prime_UTR_variant, intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10205257C>T
(R6)3R:10205424G>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10205424G>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
5_prime_UTR_variant, intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10205424G>A
(R6)3R:10205545T>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10205545T>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10205545T>C
(R6)3R:10207067A>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10207067A>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10207067A>T
(R6)3R:10207934T>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10207934T>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10207934T>G
(R6)3R:10208146T>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208146T>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208146T>G
(R6)3R:10208424C>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208424C>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208424C>A
(R6)3R:10205034T>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10205034T>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10205034T>C
(R6)3R:10205668C>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10205668C>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10205668C>G
(R6)3R:10208481G>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208481G>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208481G>T
(R6)3R:10208570G>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10208570G>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10208570G>A
(R6)3R:10211623C>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10211623C>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10211623C>T
(R6)3R:10204137T>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10204137T>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant, 3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10204137T>C
(R6)3R:10210170A>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10210170A>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10210170A>T
(R6)3R:10210600A>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10210600A>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10210600A>G
(R6)3R:10204025G>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10204025G>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant, synonymous_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10204025G>C
(R6)3R:10206713C>T
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10206713C>T
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10206713C>T
(R6)3R:10211159G>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10211159G>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10211159G>C
(R6)3R:10212388G>C
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10212388G>C
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10212388G>C
(R6)3R:10212527C>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10212527C>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10212527C>G
(R6)3R:10206096A>G
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10206096A>G
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10206096A>G
(R6)3R:10206870G>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10206870G>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10206870G>A
(R6)3R:10206879G>A
(
Drosophila melanogaster
)
Allele/Variant
Source:
NT_033777.3:g.10206879G>A
Genes:
Syn (Dme),
Timp (Dme)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(R6)3R:10206879G>A
Page 1 of 5
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