WormBase Tree Display for Variation: WBVar00277913
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WBVar00277913 | Evidence | Paper_evidence | WBPaper00036200 | ||
---|---|---|---|---|---|
Name | Public_name | gk2384 | |||
Other_name | Y54G2A.17b.1:c.889+209T>G | ||||
Y54G2A.17a.2:c.829+209T>G | |||||
Y54G2A.17a.1:c.829+209T>G | |||||
Y54G2A.17a.3:c.829+209T>G | |||||
HGVSg | CHROMOSOME_IV:g.2880500A>C | ||||
Sequence_details | SMap | S_parent | Sequence | Y54G2A | |
Flanking_sequences | AAAAAAAAATCGGGTTTTTTCGATTTTTCT | CAGGCGCCTCTCACACGTGTATCGCGTGTG | |||
Mapping_target | Y54G2A | ||||
Type_of_mutation | Substitution | A | C | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00037339 | ||||
Laboratory | VC | ||||
Person | WBPerson427 | ||||
Analysis | Million_Mutation_Pilot_Project | ||||
KO_consortium_allele | |||||
Status | Live | ||||
Affects | Gene | WBGene00021882 | |||
Transcript | Y54G2A.17a.3 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | Y54G2A.17a.3:c.829+209T>G | ||||
Intron_number | 3/7 | ||||
Y54G2A.17b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y54G2A.17b.1:c.889+209T>G | ||||
Intron_number | 4/7 | ||||
Y54G2A.17a.2 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y54G2A.17a.2:c.829+209T>G | ||||
Intron_number | 4/8 | ||||
Y54G2A.17a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y54G2A.17a.1:c.829+209T>G | ||||
Intron_number | 4/8 | ||||
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 |