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WormBase Tree Display for Variation: WBVar00271742

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Name Class

WBVar00271742NamePublic_nameWBVar00271742
Other_nameuCE5-1049
haw164354
cewivar00229734
Y39H10A.2c.1:c.721-13A>C
Y39H10A.2a.1:c.1690-13A>C
Y39H10A.2b.1:c.1696-13A>C
HGVSgCHROMOSOME_V:g.3765495A>C
Sequence_detailsSMapS_parentSequenceY39H10A
Flanking_sequencesAGATTTATATAATGGGGATGGTACTGGGATATTTCATGCGGCGAATTCCAAAAATCAACATAAACCCTGTAAGTTTTCATTCAGCCCGCCATCAGGATGAATTTATGTTCAGTGGGTCGATCGAATAATGTGGTGCTTATCCTTAGGATCCATGATTTTCGTTATTGTAATTATGGAAGACTATACATCTGGCCACCTCT
Mapping_targetY39H10A
Type_of_mutationSubstitutionAC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (20)
LaboratoryQX
PersonWBPerson4037
WBPerson1730
AnalysisSNP_Swan
WGS_Yanai
Million_mutation_project_reanalysis
WGS_Andersen
HistoryAcquires_mergeWBVar01458996
WBVar00584219
StatusLive
AffectsGeneWBGene00021479
TranscriptY39H10A.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39H10A.2c.1:c.721-13A>C
Intron_number4/6
Y39H10A.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39H10A.2b.1:c.1696-13A>C
Intron_number10/12
Y39H10A.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39H10A.2a.1:c.1690-13A>C
Intron_number10/13
ReferenceWBPaper00038208
WBPaper00040707
WBPaper00005369
MethodSNP_Swan