Version: 8.0.0
Date: Tue Jan 28 2025
42 results
Allele/Variant Genes: W01F3.2 (Cel)

(WBcel235)V:20660980T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660980T>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660980T>A

(WBcel235)V:20661743G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661743G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661743G>A

(WBcel235)V:20660965G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660965G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660965G>A

(WBcel235)V:20661596A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661596A>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661596A>T

(WBcel235)V:20661733C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661733C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661733C>T

(WBcel235)V:20661780T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661780T>C
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661780T>C

(WBcel235)V:20660634G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660634G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660634G>A

(WBcel235)V:20661679C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661679C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661679C>T

(WBcel235)V:20661753T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661753T>G
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661753T>G

(WBcel235)V:20661889A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661889A>G
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661889A>G

(WBcel235)V:20660591G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660591G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660591G>A

(WBcel235)V:20661160G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661160G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661160G>A

(WBcel235)V:20661020C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661020C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661020C>T

(WBcel235)V:20661093C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661093C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661093C>T

(WBcel235)V:20661172G>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661172G>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661172G>T

(WBcel235)V:20660376C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660376C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660376C>T

(WBcel235)V:20660602C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660602C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660602C>T

(WBcel235)V:20661140C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661140C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661140C>T

(WBcel235)V:20661386T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661386T>C
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661386T>C

(WBcel235)V:20660734T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660734T>G
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660734T>G

(WBcel235)V:20660876C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660876C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660876C>T

(WBcel235)V:20660978T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660978T>C
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660978T>C

(WBcel235)V:20661327G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661327G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661327G>A

(WBcel235)V:20661820C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661820C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661820C>T

(WBcel235)V:20661946T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661946T>G
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661946T>G

(WBcel235)V:20661145C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661145C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661145C>T

(WBcel235)V:20661835G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661835G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661835G>A

(WBcel235)V:20660676G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660676G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660676G>A

(WBcel235)V:20660695T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660695T>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660695T>A

(WBcel235)V:20661648C>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661648C>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661648C>A

(WBcel235)V:20661166G>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661166G>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661166G>T

(WBcel235)V:20661470G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661470G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661470G>A

(WBcel235)V:20661817C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661817C>T
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661817C>T

(WBcel235)V:20660719T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660719T>C
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660719T>C

(WBcel235)V:20661123A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661123A>G
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661123A>G

(WBcel235)V:20661371A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661371A>C
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661371A>C

(WBcel235)V:20661928G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661928G>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (WBcel235)V:20661928G>A

(WBcel235)V:20661019C>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661019C>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661019C>A

(WBcel235)V:20661514A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661514A>C
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661514A>C

(WBcel235)V:20660814A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20660814A>G
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20660814A>G

(WBcel235)V:20661099T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661099T>A
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661099T>A

(WBcel235)V:20661902C>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.20661902C>G
Genes: W01F3.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)V:20661902C>G