WormBase Tree Display for Variation: WBVar00277589
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WBVar00277589 | Evidence | Paper_evidence | WBPaper00036200 | ||
---|---|---|---|---|---|
Name | Public_name | gk2723 | |||
Other_name | Y18H1A.6a.1:c.1086+49C>T | ||||
Y18H1A.6b.1:c.237+49C>T | |||||
Y18H1A.6c.1:c.768+49C>T | |||||
HGVSg | CHROMOSOME_I:g.724815C>T | ||||
Sequence_details | SMap | S_parent | Sequence | Y18H1A | |
Flanking_sequences | GATCTACAAAAAATGCGGGAGTTTTCCCAG | ATTGCTCATTTGATCTACAAAAAATGCGGG | |||
Mapping_target | Y18H1A | ||||
Type_of_mutation | Substitution | C | T | ||
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 | WBGene00004028 | |||
Transcript | Y18H1A.6c.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | Y18H1A.6c.1:c.768+49C>T | ||||
Intron_number | 6/10 | ||||
Y18H1A.6b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y18H1A.6b.1:c.237+49C>T | ||||
Intron_number | 2/6 | ||||
Y18H1A.6a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y18H1A.6a.1:c.1086+49C>T | ||||
Intron_number | 9/14 | ||||
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 |