17 results
Allele/Variant Genes: ceh-17 (Cel)

np1

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00091303
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

(WBcel235)I:4568916G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4568916G>A
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4568916G>A

(WBcel235)I:4568766A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4568766A>G
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4568766A>G

(WBcel235)I:4569285C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569285C>T
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569285C>T

(WBcel235)I:4569421A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569421A>C
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569421A>C

(WBcel235)I:4569208G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569208G>A
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569208G>A

(WBcel235)I:4569597C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569597C>T
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569597C>T

(WBcel235)I:4569219G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569219G>A
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569219G>A

(WBcel235)I:4569491C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569491C>T
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569491C>T

(WBcel235)I:4569973A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569973A>C
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569973A>C

(WBcel235)I:4569257G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569257G>A
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569257G>A

(WBcel235)I:4569942G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569942G>A
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569942G>A

(WBcel235)I:4569284C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569284C>T
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569284C>T

(WBcel235)I:4569206G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569206G>A
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569206G>A

(WBcel235)I:4569952C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569952C>T
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569952C>T

(WBcel235)I:4569551A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569551A>T
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569551A>T

(WBcel235)I:4569837G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.4569837G>A
Genes: ceh-17 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:4569837G>A