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WormBase Tree Display for Variation: WBVar00277222

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Name Class

WBVar00277222EvidencePaper_evidenceWBPaper00036200
NamePublic_nameok5206
Other_nameT08B2.7b.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
HGVSgCHROMOSOME_I:g.6207701T>G
Sequence_detailsSMapS_parentSequenceT08B2
Flanking_sequencesACCTTCTTGCTTCCCTTCTTTCCGTCTCCAATACAAAGATACCCTTTCCAGTTTTACGTC
Mapping_targetT08B2
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00033305
LaboratoryRB
PersonWBPerson46
AnalysisMillion_Mutation_Pilot_Project
KO_consortium_allele
StatusLive
AffectsGeneWBGene00020347
TranscriptT08B2.7a.1VEP_consequencemissense_variant
VEP_impactMODERATE
HGVScT08B2.7a.1:c.1967A>C
HGVSpCE13431:p.Tyr656Ser
cDNA_position2015
CDS_position1967
Protein_position656
Exon_number7/9
Codon_changetAt/tCt
Amino_acid_changeY/S
T08B2.7b.3VEP_consequencemissense_variant
VEP_impactMODERATE
HGVScT08B2.7b.3:c.1889A>C
HGVSpCE26950:p.Tyr630Ser
cDNA_position1893
CDS_position1889
Protein_position630
Exon_number5/7
Codon_changetAt/tCt
Amino_acid_changeY/S
T08B2.7b.1VEP_consequencemissense_variant
VEP_impactMODERATE
HGVScT08B2.7b.1:c.1889A>C
HGVSpCE26950:p.Tyr630Ser
cDNA_position1954
CDS_position1889
Protein_position630
Exon_number6/8
Codon_changetAt/tCt
Amino_acid_changeY/S
T08B2.7b.2VEP_consequencemissense_variant
VEP_impactMODERATE
HGVScT08B2.7b.2:c.1889A>C
HGVSpCE26950:p.Tyr630Ser
cDNA_position1948
CDS_position1889
Protein_position630
Exon_number6/8
Codon_changetAt/tCt
Amino_acid_changeY/S
IsolationMutagenENU
ReferenceWBPaper00036200
RemarkAllele identified through whole-genome sequencing by the Gene Knockout ConsortiumPaper_evidenceWBPaper00036200
Sequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele