WormBase Tree Display for Variation: WBVar00277222
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WBVar00277222 | Evidence | Paper_evidence | WBPaper00036200 | ||
---|---|---|---|---|---|
Name | Public_name | ok5206 | |||
Other_name | T08B2.7b.2:c.1889A>C | ||||
CE13431:p.Tyr656Ser | |||||
CE26950:p.Tyr630Ser | |||||
T08B2.7b.1:c.1889A>C | |||||
T08B2.7b.3:c.1889A>C | |||||
T08B2.7a.1:c.1967A>C | |||||
HGVSg | CHROMOSOME_I:g.6207701T>G | ||||
Sequence_details | SMap | S_parent | Sequence | T08B2 | |
Flanking_sequences | ACCTTCTTGCTTCCCTTCTTTCCGTCTCCA | ATACAAAGATACCCTTTCCAGTTTTACGTC | |||
Mapping_target | T08B2 | ||||
Type_of_mutation | Substitution | T | G | ||
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 | WBGene00020347 | |||
Transcript | T08B2.7a.1 | VEP_consequence | missense_variant | ||
VEP_impact | MODERATE | ||||
HGVSc | T08B2.7a.1:c.1967A>C | ||||
HGVSp | CE13431:p.Tyr656Ser | ||||
cDNA_position | 2015 | ||||
CDS_position | 1967 | ||||
Protein_position | 656 | ||||
Exon_number | 7/9 | ||||
Codon_change | tAt/tCt | ||||
Amino_acid_change | Y/S | ||||
T08B2.7b.3 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | T08B2.7b.3:c.1889A>C | ||||
HGVSp | CE26950:p.Tyr630Ser | ||||
cDNA_position | 1893 | ||||
CDS_position | 1889 | ||||
Protein_position | 630 | ||||
Exon_number | 5/7 | ||||
Codon_change | tAt/tCt | ||||
Amino_acid_change | Y/S | ||||
T08B2.7b.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | T08B2.7b.1:c.1889A>C | ||||
HGVSp | CE26950:p.Tyr630Ser | ||||
cDNA_position | 1954 | ||||
CDS_position | 1889 | ||||
Protein_position | 630 | ||||
Exon_number | 6/8 | ||||
Codon_change | tAt/tCt | ||||
Amino_acid_change | Y/S | ||||
T08B2.7b.2 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | ||||
HGVSc | T08B2.7b.2:c.1889A>C | ||||
HGVSp | CE26950:p.Tyr630Ser | ||||
cDNA_position | 1948 | ||||
CDS_position | 1889 | ||||
Protein_position | 630 | ||||
Exon_number | 6/8 | ||||
Codon_change | tAt/tCt | ||||
Amino_acid_change | Y/S | ||||
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 |