42 results
Allele/Variant Genes: hpk-1 (Cel) Molecular Consequence: intron variant

(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: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: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

(WBcel235)X:4216354G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216354G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216354G>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:4214464A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214464A>C
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:4214464A>C

(WBcel235)X:4215525G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215525G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215525G>A

(WBcel235)X:4213487C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4213487C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4213487C>T

(WBcel235)X:4214242A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214242A>G
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4214242A>G

(WBcel235)X:4215849G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215849G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215849G>A

(WBcel235)X:4216040G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216040G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216040G>A

(WBcel235)X:4216313A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216313A>G
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216313A>G

(WBcel235)X:4215683T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215683T>C
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215683T>C

(WBcel235)X:4216221C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216221C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216221C>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: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:4215045G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215045G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215045G>A

(WBcel235)X:4214734G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214734G>A
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:4214734G>A

(WBcel235)X:4216110C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4216110C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4216110C>T

(WBcel235)X:4214751G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214751G>A
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:4214751G>A

(WBcel235)X:4214826G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214826G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4214826G>A

(WBcel235)X:4215719T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215719T>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215719T>A

(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: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:4215672C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215672C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215672C>T

(WBcel235)X:4215325G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215325G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215325G>A

(WBcel235)X:4215644G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215644G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215644G>A

(WBcel235)X:4214838C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4214838C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4214838C>T

(WBcel235)X:4215138G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215138G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215138G>A

(WBcel235)X:4215350C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215350C>T
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215350C>T

(WBcel235)X:4215429G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.4215429G>A
Genes: hpk-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:4215429G>A