97 results
Allele/Variant Genes: hpk-1 (Cel)

(WBcel235)X:4211042G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4211042G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4211042G>A

(WBcel235)X:4213147T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4213147T>C
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4213147T>C

(WBcel235)X:4214727T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214727T>G
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4214727T>G

(WBcel235)X:4215064T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215064T>C
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215064T>C

(WBcel235)X:4215157A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215157A>C
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215157A>C

(WBcel235)X:4215457G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215457G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215457G>A

(WBcel235)X:4216115C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216115C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216115C>T

(WBcel235)X:4212476G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212476G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212476G>A

(WBcel235)X:4211810T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4211810T>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4211810T>A

(WBcel235)X:4212113A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212113A>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212113A>T

(WBcel235)X:4213200C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4213200C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4213200C>T

(WBcel235)X:4211228A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4211228A>G
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4211228A>G

(WBcel235)X:4211265G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4211265G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4211265G>A

(WBcel235)X:4212506G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212506G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212506G>A

(WBcel235)X:4213453G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4213453G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4213453G>A

(WBcel235)X:4213916C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4213916C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4213916C>T

(WBcel235)X:4214509G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214509G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4214509G>A

(WBcel235)X:4210967G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4210967G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4210967G>A

(WBcel235)X:4212577G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212577G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212577G>A

(WBcel235)X:4212979C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212979C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212979C>T

pk1393

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00239362
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant, stop_lost, splice_donor_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available

(WBcel235)X:4211801G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4211801G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4211801G>A

(WBcel235)X:4212084C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212084C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212084C>T

(WBcel235)X:4212134G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212134G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212134G>A

(WBcel235)X:4212734G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212734G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212734G>A

(WBcel235)X:4216384G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216384G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216384G>A

(WBcel235)X:4216203C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216203C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216203C>T

(WBcel235)X:4211278A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4211278A>G
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4211278A>G

(WBcel235)X:4213185G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4213185G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4213185G>A

(WBcel235)X:4217151C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4217151C>T
Genes: F20B6.10 (Cel), hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4217151C>T

(WBcel235)X:4211106A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4211106A>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4211106A>T

(WBcel235)X:4210882A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4210882A>C
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4210882A>C

(WBcel235)X:4210980G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4210980G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4210980G>A

(WBcel235)X:4217006T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4217006T>G
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4217006T>G

(WBcel235)X:4215446G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215446G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215446G>A

(WBcel235)X:4215718G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215718G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215718G>A

(WBcel235)X:4212088C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212088C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212088C>T

(WBcel235)X:4215608G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215608G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215608G>A

(WBcel235)X:4215951C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215951C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215951C>T

(WBcel235)X:4216065G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216065G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216065G>A

(WBcel235)X:4216645A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216645A>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216645A>T

(WBcel235)X:4212982A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212982A>C
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212982A>C

(WBcel235)X:4211895C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4211895C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4211895C>T

(WBcel235)X:4212795C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4212795C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4212795C>T

(WBcel235)X:4216411A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216411A>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216411A>T

(WBcel235)X:4216419C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216419C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216419C>T

(WBcel235)X:4217010G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4217010G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4217010G>A

(WBcel235)X:4217049C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4217049C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4217049C>T

(WBcel235)X:4214773G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214773G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4214773G>A

(WBcel235)X:4214781C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214781C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4214781C>T