WormBase Tree Display for Variation: WBVar00276740
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WBVar00276740 | Evidence | Paper_evidence | WBPaper00036200 | ||
---|---|---|---|---|---|
Name | Public_name | ok5094 | |||
Other_name | F56C9.3.2:c.678G>A | ||||
CE29406:p.Val226= | |||||
F56C9.3.1:c.678G>A | |||||
HGVSg | CHROMOSOME_III:g.7312111G>A | ||||
Sequence_details | SMap | S_parent | Sequence | F56C9 | |
Flanking_sequences | GGCAAGTGTACAGCTTATTATCTCCTCAGT | AGAAGAATCCATGACGCAGGTGCGAATCTT | |||
Mapping_target | F56C9 | ||||
Type_of_mutation | Substitution | G | A | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00033304 | ||||
Laboratory | RB | ||||
Person | WBPerson46 | ||||
Analysis | Million_Mutation_Pilot_Project | ||||
KO_consortium_allele | |||||
Status | Live | ||||
Affects | Gene | WBGene00018948 | |||
Transcript | F56C9.3.2 | VEP_consequence | synonymous_variant | ||
VEP_impact | LOW | ||||
HGVSc | F56C9.3.2:c.678G>A | ||||
HGVSp | CE29406:p.Val226= | ||||
cDNA_position | 709 | ||||
CDS_position | 678 | ||||
Protein_position | 226 | ||||
Exon_number | 4/8 | ||||
Codon_change | gtG/gtA | ||||
Amino_acid_change | V | ||||
F56C9.3.1 | VEP_consequence | synonymous_variant | |||
VEP_impact | LOW | ||||
HGVSc | F56C9.3.1:c.678G>A | ||||
HGVSp | CE29406:p.Val226= | ||||
cDNA_position | 716 | ||||
CDS_position | 678 | ||||
Protein_position | 226 | ||||
Exon_number | 4/8 | ||||
Codon_change | gtG/gtA | ||||
Amino_acid_change | V | ||||
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 |