15 results
Allele/Variant Genes: W01F3.2 (Cel) Molecular Consequence: missense variant

(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: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: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: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: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: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: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: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: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: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: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