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WormBase Tree Display for Variation: WBVar01258670

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Name Class

WBVar01258670EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01258670
Other_namecewivar00148607
M01E10.2b.1:c.1354-201T>C
M01E10.2a.1:c.2353-201T>C
HGVSgCHROMOSOME_III:g.2041163A>G
Sequence_detailsSMapS_parentSequenceM01E10
Flanking_sequencesGCCTTTAATTTCGTGGTGGGACCCAAATTTTGAAAACAGTCGGAACCTAGCATGATGGGTGTCATTTGAAAGCTCATATCGTGCTGAATTTGAAAATGTT
Mapping_targetM01E10
Type_of_mutationSubstitutionaGPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539094747
StatusLive
AffectsGeneWBGene00001063
TranscriptM01E10.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM01E10.2a.1:c.2353-201T>C
Intron_number11/21
M01E10.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM01E10.2b.1:c.1354-201T>C
Intron_number6/16
ReferenceWBPaper00037807
MethodWGS_De_Bono