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WormBase Tree Display for Variation: WBVar01241664

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Name Class

WBVar01241664EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01241664
Other_namecewivar00139486
F18A1.3b.1:c.66+2910T>C
F18A1.3a.1:c.66+2910T>C
F18A1.3l.1:c.66+2910T>C
F18A1.3c.1:c.66+2910T>C
F18A1.3i.1:c.66+2910T>C
F18A1.3d.1:c.66+2910T>C
HGVSgCHROMOSOME_II:g.7675018T>C
Sequence_detailsSMapS_parentSequenceF18A1
Flanking_sequencesCGCTCTATAAATCGACCCCGATTGGAGCCAATTCAGATGAAATCGTTTTGGCGCACACACGCTTGTCTAAATCGGATTCGTTCTACCAACGTGATTCACT
Mapping_targetF18A1
Type_of_mutationSubstitutiontCPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (18)
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539079442
HistoryAcquires_mergeWBVar01308111
StatusLive
AffectsGeneWBGene00003044
TranscriptF18A1.3l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3l.1:c.66+2910T>C
Intron_number2/6
F18A1.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3b.1:c.66+2910T>C
Intron_number2/6
F18A1.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3a.1:c.66+2910T>C
Intron_number2/5
F18A1.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3c.1:c.66+2910T>C
Intron_number2/4
F18A1.3i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3i.1:c.66+2910T>C
Intron_number2/6
F18A1.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3d.1:c.66+2910T>C
Intron_number2/6
ReferenceWBPaper00037807
MethodWGS_De_Bono