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WormBase Tree Display for Variation: WBVar01264312

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Name Class

WBVar01264312EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01264312
Other_namecewivar00150664
F47D12.1a.1:c.157-1251T>C
F47D12.1d.1:c.157-1251T>C
F47D12.1c.1:c.157-1251T>C
F47D12.1b.1:c.157-1251T>C
HGVSgCHROMOSOME_III:g.6312945T>C
Sequence_detailsSMapS_parentSequenceF47D12
Flanking_sequencesTTCTCTTTGGCACAGATTTTCCCGAGCACGGTATCTCTGTAGTCTTGATATTTTTTTTCAATTCTCGACCTTCTTTTCCTCTCATTCTGTTGTAAACCGA
Mapping_targetF47D12
Type_of_mutationSubstitutiontCPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (20)
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539099825
StatusLive
AffectsGeneWBGene00001518
TranscriptF47D12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1d.1:c.157-1251T>C
Intron_number1/4
F47D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1b.1:c.157-1251T>C
Intron_number2/12
F47D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1a.1:c.157-1251T>C
Intron_number2/13
F47D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1c.1:c.157-1251T>C
Intron_number2/12
ReferenceWBPaper00037807
MethodWGS_De_Bono