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WormBase Tree Display for Variation: WBVar00271673

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Name Class

WBVar00271673EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00271673
Other_nameuCE5-964
cewivar00228696
F27E11.3.1:c.367C>T
CE39149:p.Leu123=
HGVSgCHROMOSOME_V:g.3443857G>A
Sequence_detailsSMapS_parentSequenceF27E11
Flanking_sequencesTGATGCCCCTTGTGCTGCTTCTTTGGTGTATCTGGTGGAGCTGCACAGATGTTCCCAGTCGACATCTGATCCGACATCTTTGGCAGCGCCTCGCAAGACATGTCTCGGGCCATCTGAATCCGTACTTGGCCATTATTGGACTGCACTTGCTGCGTGCCTCCACACAAAGTTCCATGCACGGGAGAATTGGTTTGTCGTAG
Mapping_targetF27E11
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
AnalysisSNP_Swan
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000478
TranscriptF27E11.3.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF27E11.3.1:c.367C>T
HGVSpCE39149:p.Leu123=
cDNA_position369
CDS_position367
Protein_position123
Exon_number3/6
Codon_changeCtg/Ttg
Amino_acid_changeL
ReferenceWBPaper00005369
MethodSNP_Swan