Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: T12D8.9 (Cel)
(WBcel235)III:13618559C>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618559C>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618559C>A
(WBcel235)III:13621133C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13621133C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13621133C>T
(WBcel235)III:13620110C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620110C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620110C>T
(WBcel235)III:13620290C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620290C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620290C>T
(WBcel235)III:13621277A>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13621277A>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13621277A>T
(WBcel235)III:13617191C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617191C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617191C>T
(WBcel235)III:13617355C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617355C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617355C>T
(WBcel235)III:13618526A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618526A>G
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618526A>G
(WBcel235)III:13619386A>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619386A>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619386A>T
(WBcel235)III:13619726A>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619726A>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619726A>T
(WBcel235)III:13619126C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619126C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619126C>T
(WBcel235)III:13618734G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618734G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618734G>A
(WBcel235)III:13620056C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620056C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620056C>T
(WBcel235)III:13621137C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13621137C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13621137C>T
(WBcel235)III:13618296C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618296C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618296C>T
(WBcel235)III:13618228A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618228A>G
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618228A>G
(WBcel235)III:13620814A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620814A>G
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620814A>G
(WBcel235)III:13620859G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620859G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620859G>A
(WBcel235)III:13619178G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619178G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619178G>A
(WBcel235)III:13619306G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619306G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619306G>A
(WBcel235)III:13617714G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617714G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617714G>A
(WBcel235)III:13617898C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617898C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617898C>T
(WBcel235)III:13620564G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620564G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620564G>A
(WBcel235)III:13620222C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620222C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620222C>T
(WBcel235)III:13619575C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619575C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619575C>T
(WBcel235)III:13620728G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620728G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620728G>A
(WBcel235)III:13620789A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620789A>G
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620789A>G
(WBcel235)III:13617866G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617866G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617866G>A
(WBcel235)III:13619319G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619319G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619319G>A
(WBcel235)III:13617375T>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617375T>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617375T>A
(WBcel235)III:13617678C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617678C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617678C>T
(WBcel235)III:13617577T>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617577T>G
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617577T>G
(WBcel235)III:13619467G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619467G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619467G>A
(WBcel235)III:13621277A>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13621277A>C
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13621277A>C
(WBcel235)III:13620494T>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620494T>C
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620494T>C
(WBcel235)III:13619025T>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619025T>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619025T>A
(WBcel235)III:13619522G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619522G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619522G>A
(WBcel235)III:13618479G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618479G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618479G>A
(WBcel235)III:13620643A>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620643A>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620643A>T
(WBcel235)III:13619031C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619031C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619031C>T
(WBcel235)III:13617301C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617301C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617301C>T
(WBcel235)III:13618332G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618332G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618332G>A
(WBcel235)III:13619322G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619322G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619322G>A
(WBcel235)III:13620942G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13620942G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13620942G>A
(WBcel235)III:13619814C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619814C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619814C>T
(WBcel235)III:13617992C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13617992C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13617992C>T
(WBcel235)III:13619045G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619045G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619045G>A
(WBcel235)III:13619755C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13619755C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13619755C>T
(WBcel235)III:13618036C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618036C>T
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618036C>T
(WBcel235)III:13618878G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003281.10:g.13618878G>A
Genes: hip-1 (Cel), T12D8.9 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:13618878G>A