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
Caenorhabditis elegans
17
×
Category
variant
17
×
Variant Type
SNP
17
×
Molecular Consequence
missense variant
7
×
synonymous variant
4
×
3 prime UTR variant
3
×
intron variant
2
×
stop retained variant
1
×
Genes
C29F7.3 (Cel)
17
×
Filter
17
results
Page 1 of 1
Allele/Variant
Genes: C29F7.3 (Cel)
Molecular Consequence:
stop gained
(WBcel235)X:13419399C>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419399C>A
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419399C>A
(WBcel235)X:13419030C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419030C>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
stop_retained_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419030C>T
(WBcel235)X:13419215C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419215C>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419215C>T
(WBcel235)X:13419564C>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419564C>A
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419564C>A
(WBcel235)X:13419050C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419050C>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419050C>T
(WBcel235)X:13419212G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419212G>A
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419212G>A
(WBcel235)X:13419352C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419352C>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419352C>T
(WBcel235)X:13419456G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419456G>A
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419456G>A
(WBcel235)X:13418979G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13418979G>A
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13418979G>A
(WBcel235)X:13419252A>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419252A>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419252A>T
(WBcel235)X:13419765C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419765C>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419765C>T
(WBcel235)X:13419424C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419424C>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419424C>T
(WBcel235)X:13419622A>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419622A>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419622A>T
(WBcel235)X:13419759A>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419759A>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419759A>T
(WBcel235)X:13418923G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13418923G>A
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13418923G>A
(WBcel235)X:13419293C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13419293C>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13419293C>T
(WBcel235)X:13418954C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003284.9:g.13418954C>T
Genes:
C29F7.3 (Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(WBcel235)X:13418954C>T
Page 1 of 1
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