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WormBase Tree Display for Variation: WBVar01421172

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Name Class

WBVar01421172EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01421172
Other_namecewivar00278226
Y54E10BR.7.1:c.981T>C
CE28995:p.Leu327=
HGVSgCHROMOSOME_I:g.3041946A>G
Sequence_detailsSMapS_parentSequenceY54E10BR
Flanking_sequencesTTCTCGAAATCCGGTGTCACATAATAATAGAGACCATTCTTTGCTCCAGGAGAAGAAGTCCACGTATAAGAAGAATACTTAGAATAATATATGGAGCTGT
Mapping_targetY54E10BR
Type_of_mutationSubstitutionaGPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539128507
StatusLive
AffectsGeneWBGene00003387
TranscriptY54E10BR.7.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScY54E10BR.7.1:c.981T>C
HGVSpCE28995:p.Leu327=
cDNA_position981
CDS_position981
Protein_position327
Exon_number7/13
Codon_changectT/ctC
Amino_acid_changeL
ReferenceWBPaper00037807
MethodWGS_De_Bono