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WormBase Tree Display for Variation: WBVar00558543

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Name Class

WBVar00558543NamePublic_nameWBVar00558543
Other_namehaw138678
cewivar00191053
C29F9.6.1:c.546T>C
C29F9.6.2:c.546T>C
CE43673:p.Ser182=
C29F9.6.3:c.546T>C
HGVSgCHROMOSOME_III:g.116270T>C
Sequence_detailsSMapS_parentSequenceC29F9
Flanking_sequencesAAGGAGGACGCGAGGGCTGCTGAGCTTCAGATTTTTGAAGCAGCGGGGAGAGGGATGAGTACTACCGCATGGTTGAGGAGCGAGCTCCCCGCGAGCAGGA
Mapping_targetC29F9
Type_of_mutationSubstitutiontc
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisWGS_De_Bono
WGS_Yanai
Million_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
PersonWBPerson4037
AnalysisWGS_Yanai
WGS_De_Bono
Million_mutation_project_reanalysis
HistoryAcquires_mergeWBVar01387907
StatusLive
AffectsGeneWBGene00016221
TranscriptC29F9.6.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.6.1:c.546T>C
HGVSpCE43673:p.Ser182=
cDNA_position718
CDS_position546
Protein_position182
Exon_number7/9
Codon_changeagT/agC
Amino_acid_changeS
C29F9.6.3VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.6.3:c.546T>C
HGVSpCE43673:p.Ser182=
cDNA_position641
CDS_position546
Protein_position182
Exon_number6/8
Codon_changeagT/agC
Amino_acid_changeS
C29F9.6.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC29F9.6.2:c.546T>C
HGVSpCE43673:p.Ser182=
cDNA_position693
CDS_position546
Protein_position182
Exon_number5/7
Codon_changeagT/agC
Amino_acid_changeS
ReferenceWBPaper00038208
WBPaper00037807
MethodWGS_Yanai