WormBase Tree Display for Variation: WBVar00277164
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WBVar00277164 | Evidence | Paper_evidence | WBPaper00036200 | ||
---|---|---|---|---|---|
Name | Public_name | ok5248 | |||
Other_name | T02G5.15.3:c.-1590C>T | ||||
T02G5.14.1:c.-853+1177C>T | |||||
T02G5.15.2:c.-202+1177C>T | |||||
T02G5.15.1:c.-29+1177C>T | |||||
HGVSg | CHROMOSOME_II:g.7085771C>T | ||||
Sequence_details | SMap | S_parent | Sequence | T02G5 | |
Flanking_sequences | TTTGTGGGACTTCAAATTTACTGAGAAAAA | TTTTTTTGCGAGAAATTAAAATTTTCTGAG | |||
Mapping_target | T02G5 | ||||
Type_of_mutation | Substitution | C | T | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00033305 | ||||
Laboratory | RB | ||||
Person | WBPerson46 | ||||
Analysis | Million_Mutation_Pilot_Project | ||||
KO_consortium_allele | |||||
Status | Live | ||||
Affects | Gene | WBGene00020170 | |||
WBGene00206521 | |||||
Transcript | T02G5.15.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | T02G5.15.1:c.-29+1177C>T | ||||
Intron_number | 1/6 | ||||
T02G5.15.3 | VEP_consequence | 5_prime_UTR_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T02G5.15.3:c.-1590C>T | ||||
cDNA_position | 512 | ||||
Exon_number | 1/5 | ||||
T02G5.15.2 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T02G5.15.2:c.-202+1177C>T | ||||
Intron_number | 1/5 | ||||
T02G5.14.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T02G5.14.1:c.-853+1177C>T | ||||
Intron_number | 1/6 | ||||
Isolation | Mutagen | ENU | |||
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 |