WormBase Tree Display for Variation: WBVar00277135
expand all nodes | collapse all nodes | view schema
WBVar00277135 | Evidence | Paper_evidence | WBPaper00036200 | ||
---|---|---|---|---|---|
Name | Public_name | gk2822 | |||
Other_name | R166.5b.3:c.127+1411C>T | ||||
R166.5b.1:c.127+1411C>T | |||||
R166.5b.2:c.127+1411C>T | |||||
HGVSg | CHROMOSOME_II:g.10552085G>A | ||||
Sequence_details | SMap | S_parent | Sequence | R166 | |
Flanking_sequences | TCGCGTTCAATTTTTCGCCAACTAGCTGAT | ATCACATGATTCGAATGGTTAAACAGGGAA | |||
Mapping_target | R166 | ||||
Type_of_mutation | Substitution | G | A | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00005866 | ||||
Laboratory | VC | ||||
Person | WBPerson427 | ||||
Analysis | Million_Mutation_Pilot_Project | ||||
KO_consortium_allele | |||||
Status | Live | ||||
Affects | Gene | WBGene00011304 | |||
Transcript | R166.5b.2 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | R166.5b.2:c.127+1411C>T | ||||
Intron_number | 3/9 | ||||
R166.5b.3 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | R166.5b.3:c.127+1411C>T | ||||
Intron_number | 2/8 | ||||
R166.5b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | R166.5b.1:c.127+1411C>T | ||||
Intron_number | 3/9 | ||||
Isolation | Mutagen | EMS | |||
Reference | WBPaper00036200 | ||||
Remark | Allele identified through whole-genome sequencing by the Gene Knockout Consortium | Paper_evidence | WBPaper00036200 | ||
Sequenced by the C. elegans Gene Knockout Consortium | Paper_evidence | WBPaper00041807 | |||
Method | KO_consortium_allele |