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WormBase Tree Display for Variation: WBVar01472962

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Name Class

WBVar01472962EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01472962
Other_namecewivar00617411
C02C6.2a.1:c.45-383C>T
HGVSgCHROMOSOME_X:g.15542815C>T
Sequence_detailsSMapS_parentSequenceC02C6
Flanking_sequencesGTTTTACTAATTCGATTAGAAACTGAATTCCGATTTTTTTTTATCTCTCTCCCTCTCTCT
Mapping_targetC02C6
Type_of_mutationSubstitutionct
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022867From_analysisWGS_Andersen
WBStrain00022869From_analysisWGS_Andersen
WBStrain00022870From_analysisWGS_Andersen
WBStrain00022872From_analysisWGS_Andersen
WBStrain00022873From_analysisWGS_Andersen
WBStrain00022874From_analysisWGS_Andersen
WBStrain00022877From_analysisWGS_Andersen
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193358264
dbSNP_ssss295534183
StatusLive
AffectsGeneWBGene00007260
TranscriptC02C6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC02C6.2a.1:c.45-383C>T
Intron_number2/8
ReferenceWBPaper00040707
MethodWGS_Andersen