22 results
Allele/Variant Genes: nhr-69 (Cel)

(WBcel235)I:9880769G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880769G>A
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880769G>A

(WBcel235)I:9879258C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9879258C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9879258C>T

(WBcel235)I:9880498C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880498C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880498C>T

(WBcel235)I:9880216C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880216C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880216C>T

(WBcel235)I:9880383C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880383C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880383C>T

(WBcel235)I:9879260G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9879260G>A
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9879260G>A

(WBcel235)I:9879707C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9879707C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9879707C>T

(WBcel235)I:9881096C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9881096C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9881096C>T

(WBcel235)I:9881217A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9881217A>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9881217A>T

(WBcel235)I:9880051G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880051G>A
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880051G>A

(WBcel235)I:9879282A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9879282A>C
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9879282A>C

(WBcel235)I:9881310C>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9881310C>A
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9881310C>A

(WBcel235)I:9879294G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9879294G>A
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9879294G>A

(WBcel235)I:9880408C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880408C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880408C>T

(WBcel235)I:9881282C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9881282C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9881282C>T

(WBcel235)I:9881343T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9881343T>C
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9881343T>C

(WBcel235)I:9879966C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9879966C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9879966C>T

(WBcel235)I:9880833G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880833G>A
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880833G>A

(WBcel235)I:9880977T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880977T>A
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880977T>A

(WBcel235)I:9880169G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880169G>A
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880169G>A

(WBcel235)I:9880391C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9880391C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9880391C>T

(WBcel235)I:9881484C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003279.8:g.9881484C>T
Genes: nhr-69 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:9881484C>T