WormBase Tree Display for Variation: WBVar00143836
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WBVar00143836 | Evidence | Paper_evidence | WBPaper00000779 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | e1213 | |||||
Other_name | CE09349:p.Gln1663Ter | ||||||
F11C3.3.1:c.4987C>T | |||||||
HGVSg | CHROMOSOME_I:g.14857241G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | F32A7 | |||
Flanking_sequences | aagagataccaagagcaagtccgcgagttg | aattgcaagtcgaggaggagcaacgcaatg | |||||
Mapping_target | F32A7 | ||||||
Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00000779 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00033518 | ||||||
WBStrain00033524 | |||||||
Laboratory | CB | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00006789 | |||||
Transcript | F11C3.3.1 | VEP_consequence | stop_gained | ||||
VEP_impact | HIGH | ||||||
HGVSc | F11C3.3.1:c.4987C>T | ||||||
HGVSp | CE09349:p.Gln1663Ter | ||||||
cDNA_position | 5019 | ||||||
CDS_position | 4987 | ||||||
Protein_position | 1663 | ||||||
Exon_number | 7/11 | ||||||
Codon_change | Caa/Taa | ||||||
Amino_acid_change | Q/* | ||||||
Isolation | Mutagen | EMS | Paper_evidence | WBPaper00000779 | |||
Genetics | Interpolated_map_position | I | 27.9601 | ||||
Mapping_data | In_2_point | 7014 | |||||
In_multi_point | 3094 | ||||||
3095 | |||||||
Reference | WBPaper00016080 | ||||||
Method | Substitution_allele |