Version: 8.0.0
Date: Tue Jan 28 2025
7 results
Allele/Variant Genes: fubl-1 (Cel) Molecular Consequence: 5 prime UTR variant

(WBcel235)V:10238774G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.10238774G>A
Genes: fubl-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)V:10238774G>A

(WBcel235)V:10238743G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.10238743G>A
Genes: fubl-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:10238743G>A

(WBcel235)V:10238770C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.10238770C>T
Genes: fubl-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)V:10238770C>T

(WBcel235)V:10238852C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.10238852C>T
Genes: fubl-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)V:10238852C>T

(WBcel235)V:10238723A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.10238723A>T
Genes: fubl-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:10238723A>T

(WBcel235)V:10238817C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.10238817C>T
Genes: fubl-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)V:10238817C>T

(WBcel235)V:10238390G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.10238390G>A
Genes: fubl-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:10238390G>A