WormBase Tree Display for Variation: WBVar00277202
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WBVar00277202 | Evidence | Paper_evidence | WBPaper00036200 | ||
---|---|---|---|---|---|
Name | Public_name | ok5875 | |||
Other_name | T06F4.1e.1:c.27-6444G>A | ||||
T06F4.1c.1:c.53+3918G>A | |||||
T06F4.1a.1:c.53+3918G>A | |||||
HGVSg | CHROMOSOME_X:g.4067479C>T | ||||
Sequence_details | SMap | S_parent | Sequence | T06F4 | |
Flanking_sequences | AAAAATGTTCTGAAAATTAATATTGCACTC | CTATTAGTCTTGCACTCCCTATTAGTATTG | |||
Mapping_target | T06F4 | ||||
Type_of_mutation | Substitution | C | T | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00033306 | ||||
Laboratory | RB | ||||
Person | WBPerson46 | ||||
Analysis | Million_Mutation_Pilot_Project | ||||
KO_consortium_allele | |||||
Status | Live | ||||
Affects | Gene | WBGene00020294 | |||
Transcript | T06F4.1e.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | T06F4.1e.1:c.27-6444G>A | ||||
Intron_number | 1/6 | ||||
T06F4.1a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T06F4.1a.1:c.53+3918G>A | ||||
Intron_number | 2/7 | ||||
T06F4.1c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T06F4.1c.1:c.53+3918G>A | ||||
Intron_number | 2/8 | ||||
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 |