Version: 8.0.0
Date: Tue Jan 28 2025
36 results
Allele/Variant Genes: C17H12.2 (Cel)

(WBcel235)IV:6787099G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787099G>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787099G>A

(WBcel235)IV:6787396C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787396C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787396C>T

(WBcel235)IV:6788692A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788692A>G
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788692A>G

(WBcel235)IV:6787315A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787315A>G
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787315A>G

(WBcel235)IV:6787672A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787672A>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787672A>T

(WBcel235)IV:6789471C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6789471C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6789471C>T

(WBcel235)IV:6789877G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6789877G>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6789877G>A

(WBcel235)IV:6788562C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788562C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788562C>T

(WBcel235)IV:6788632G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788632G>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (WBcel235)IV:6788632G>A

(WBcel235)IV:6788935G>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788935G>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788935G>T

(WBcel235)IV:6786971T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6786971T>C
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6786971T>C

(WBcel235)IV:6788036C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788036C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788036C>T

(WBcel235)IV:6789236A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6789236A>C
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6789236A>C

(WBcel235)IV:6790140G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6790140G>A
Genes: C17H12.33 (Cel), C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6790140G>A

(WBcel235)IV:6790142A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6790142A>C
Genes: C17H12.33 (Cel), C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6790142A>C

(WBcel235)IV:6786943C>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6786943C>G
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6786943C>G

(WBcel235)IV:6788443C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788443C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788443C>T

(WBcel235)IV:6788967A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788967A>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788967A>T

(WBcel235)IV:6789672C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6789672C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6789672C>T

(WBcel235)IV:6787370G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787370G>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787370G>A

(WBcel235)IV:6787774G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787774G>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787774G>A

(WBcel235)IV:6788563C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788563C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788563C>T

(WBcel235)IV:6788717G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788717G>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788717G>A

(WBcel235)IV:6789599C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6789599C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6789599C>T

(WBcel235)IV:6790204G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6790204G>A
Genes: C17H12.33 (Cel), C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6790204G>A

(WBcel235)IV:6787813A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787813A>G
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787813A>G

(WBcel235)IV:6786889G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6786889G>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6786889G>A

(WBcel235)IV:6787751C>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787751C>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787751C>A

(WBcel235)IV:6787552C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787552C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (WBcel235)IV:6787552C>T

(WBcel235)IV:6789212C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6789212C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6789212C>T

(WBcel235)IV:6789983G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6789983G>A
Genes: C17H12.2 (Cel), C17H12.30 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6789983G>A

(WBcel235)IV:6788502G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6788502G>A
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6788502G>A

(WBcel235)IV:6790155G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6790155G>A
Genes: C17H12.33 (Cel), C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6790155G>A

(WBcel235)IV:6790463A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6790463A>G
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6790463A>G

(WBcel235)IV:6787980A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6787980A>G
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6787980A>G

(WBcel235)IV:6789832C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.6789832C>T
Genes: C17H12.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:6789832C>T