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WormBase Tree Display for Variation: WBVar00590556

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Name Class

WBVar00590556EvidencePaper_evidenceWBPaper00038208
NamePublic_nameWBVar00590556
Other_namehaw170691
cewivar00243608
C56A3.7a.1:c.673-176A>T
C56A3.7c.1:c.100-176A>T
C56A3.7b.1:c.577-176A>T
C56A3.7d.1:c.463-176A>T
HGVSgCHROMOSOME_V:g.13559148A>T
Sequence_detailsSMapS_parentSequenceC56A3
Flanking_sequencesGTACCTATTTACATACTTGCCTTGGGTATAAGTTTGAATAAAAAACATGTAGCCATAATGCGACCTAAGGCAGAGCTCTGCCTACCTCCACAAGTTGAAA
Mapping_targetC56A3
Type_of_mutationSubstitutionat
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WGS_Yanai
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
PersonWBPerson4037
AnalysisWGS_Yanai
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000302
TranscriptC56A3.7a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC56A3.7a.1:c.673-176A>T
Intron_number8/11
C56A3.7d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC56A3.7d.1:c.463-176A>T
Intron_number5/7
C56A3.7b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC56A3.7b.1:c.577-176A>T
Intron_number6/8
C56A3.7c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC56A3.7c.1:c.100-176A>T
Intron_number1/3
ReferenceWBPaper00038208
MethodWGS_Yanai