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WormBase Tree Display for Variation: WBVar01446932

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Name Class

WBVar01446932EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01446932
Other_nameC29E4.1.1:c.165T>C
CE00083:p.Leu55=
HGVSgCHROMOSOME_III:g.7949054T>C
Sequence_detailsSMapS_parentSequenceC29E4
Flanking_sequencesAGTATTAGCTGATGACACGTGGCAACGTCTCTTGTTCTTCAATCCCCAACTGGAGAAACT
Mapping_targetC29E4
Type_of_mutationSubstitutiontc
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00023665From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00027648From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00027660From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00027661From_analysisWGS_Andersen
WBStrain00027662From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00027669From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193333561
dbSNP_ssss295509480
StatusLive
AffectsGeneWBGene00000665
TranscriptC29E4.1.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29E4.1.1:c.165T>C
HGVSpCE00083:p.Leu55=
cDNA_position217
CDS_position165
Protein_position55
Exon_number2/4
Codon_changectT/ctC
Amino_acid_changeL
ReferenceWBPaper00040707
MethodWGS_Andersen