WormBase Tree Display for Variation: WBVar00276662
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WBVar00276662 | Evidence | Paper_evidence | WBPaper00036200 | ||
---|---|---|---|---|---|
Name | Public_name | gk2923 | |||
Other_name | F53A2.8a.1:c.1431+46G>A | ||||
F53A2.8b.1:c.1749+46G>A | |||||
F53A2.8c.1:c.1425+46G>A | |||||
HGVSg | CHROMOSOME_III:g.13354570G>A | ||||
Sequence_details | SMap | S_parent | Sequence | F53A2 | |
Flanking_sequences | TCTGAAAATTAAATTCTGAAAATGCGTATT | CACAACATGTTTGACGCGCAAAATATCTCA | |||
Mapping_target | F53A2 | ||||
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 | WBGene00003478 | |||
Transcript | F53A2.8c.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | F53A2.8c.1:c.1425+46G>A | ||||
Intron_number | 7/9 | ||||
F53A2.8b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53A2.8b.1:c.1749+46G>A | ||||
Intron_number | 7/9 | ||||
F53A2.8a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F53A2.8a.1:c.1431+46G>A | ||||
Intron_number | 7/9 | ||||
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 |