Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: C38C5.1 (Cel)
(WBcel235)X:5560544C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560544C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560544C>T
(WBcel235)X:5560410G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560410G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560410G>A
(WBcel235)X:5560733C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560733C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560733C>T
(WBcel235)X:5561328T>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5561328T>C
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_lost
Diseases: Not Available
Variant Name: (WBcel235)X:5561328T>C
(WBcel235)X:5558303C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558303C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558303C>T
(WBcel235)X:5560992A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560992A>G
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560992A>G
(WBcel235)X:5560794G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560794G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560794G>A
(WBcel235)X:5560782C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560782C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560782C>T
(WBcel235)X:5558140C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558140C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558140C>T
(WBcel235)X:5559692C>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559692C>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559692C>A
(WBcel235)X:5560267A>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560267A>C
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560267A>C
(WBcel235)X:5558665A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558665A>G
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558665A>G
(WBcel235)X:5560693G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560693G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560693G>A
(WBcel235)X:5558701C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558701C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558701C>T
(WBcel235)X:5561131A>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5561131A>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5561131A>T
(WBcel235)X:5559090G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559090G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559090G>A
(WBcel235)X:5559671G>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559671G>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559671G>T
(WBcel235)X:5558151C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558151C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (WBcel235)X:5558151C>T
(WBcel235)X:5558382C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558382C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558382C>T
(WBcel235)X:5560407C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560407C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560407C>T
(WBcel235)X:5560951G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560951G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560951G>A
(WBcel235)X:5561260G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5561260G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5561260G>A
(WBcel235)X:5558507C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558507C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558507C>T
(WBcel235)X:5558666C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558666C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558666C>T
(WBcel235)X:5559671G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559671G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559671G>A
(WBcel235)X:5559688A>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559688A>C
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559688A>C
(WBcel235)X:5558090G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558090G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558090G>A
(WBcel235)X:5560392T>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560392T>C
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560392T>C
(WBcel235)X:5558143G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558143G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558143G>A
(WBcel235)X:5558266C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558266C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558266C>T
(WBcel235)X:5558334C>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558334C>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558334C>A
(WBcel235)X:5560585G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560585G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560585G>A
(WBcel235)X:5559986G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559986G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559986G>A
(WBcel235)X:5558803G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558803G>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558803G>A
(WBcel235)X:5558892A>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558892A>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558892A>T
(WBcel235)X:5559213C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559213C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559213C>T
(WBcel235)X:5559964C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559964C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559964C>T
(WBcel235)X:5559117G>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559117G>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559117G>T
(WBcel235)X:5559452T>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559452T>C
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559452T>C
(WBcel235)X:5560942C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560942C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560942C>T
(WBcel235)X:5561092C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5561092C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5561092C>T
(WBcel235)X:5558413G>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558413G>C
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558413G>C
(WBcel235)X:5558313C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558313C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558313C>T
(WBcel235)X:5561154C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5561154C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5561154C>T
(WBcel235)X:5558519C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5558519C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5558519C>T
(WBcel235)X:5559126T>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5559126T>A
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5559126T>A
(WBcel235)X:5560358C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560358C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560358C>T
(WBcel235)X:5560491C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003284.9:g.5560491C>T
Genes: C38C5.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:5560491C>T