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WormBase Tree Display for Variation: WBVar00051767

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Name Class

WBVar00051767NamePublic_nameWBVar00051767
Other_nameCE1-167
haw6668
cewivar00165901
F28B3.4i.1:c.627+146T>A
F28B3.4b.1:c.705+146T>A
F28B3.4j.1:c.627+146T>A
F28B3.4g.1:c.705+146T>A
HGVSgCHROMOSOME_I:g.4939124T>A
Sequence_detailsSMapS_parentSequenceF28B3
Flanking_sequencesactgcagaacgacgtgctgctgctgcttcaggtggtggtacaaggaaagaacgagctgtagaggatatgcttcgacttgttcaagagaatcgagatcggcatgatgtgagttttcgaattttaaattttgtgtaaaaaacagagtttgtttttttctcattttttgggaaactattatcaaaattccaactttaaaaaaccacaggaataaattttttaaattttatttttcattagacctaccaactttaaaaaaacttgaaaatacgagacgaacagcgaaatcgctggcatctagataaatattttaacatttggattttaataaatttaggaagtagagtaacgttaatattttttctttcctttctgaaaaaatttgcaaaaaatgttcaaatggctaattggaagagaaaaccattttaaacgtttcccaaaaaaaatctttgaattttggcgataaacgttcagattttttttttgcaaaattgaaaaaaaca
Mapping_targetF28B3
Type_of_mutationSubstitutionta
SeqStatusSequenced
Variation_typeSNP
Confirmed_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
WGS_De_Bono
WGS_Hawaiian_Waterston
Million_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisWGS_De_Bono
Million_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
RW
PersonWBPerson1562
AnalysisSNP_Swan
WGS_De_Bono
Million_mutation_project_reanalysis
WGS_Hawaiian_Waterston
HistoryAcquires_mergeWBVar00153418
WBVar01344165
WBVar01282619
StatusLive
AffectsGeneWBGene00305377
WBGene00017885
TranscriptF28B3.4g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF28B3.4g.1:c.705+146T>A
Intron_number6/17
F28B3.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF28B3.4b.1:c.705+146T>A
Intron_number6/17
F28B3.4j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF28B3.4j.1:c.627+146T>A
Intron_number3/13
F28B3.4i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF28B3.4i.1:c.627+146T>A
Intron_number3/13
F28B3.12
ReferenceWBPaper00037807
WBPaper00005369
MethodSNP_Swan