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WormBase Tree Display for Variation: WBVar02133692

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Name Class

WBVar02133692EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh8951
Other_nameW02C12.3i.1:c.214-4107G>A
W02C12.3e.1:c.187-4107G>A
W02C12.3d.1:c.187-4107G>A
W02C12.3j.1:c.214-4107G>A
W02C12.3d.2:c.187-4107G>A
W02C12.3c.1:c.367-4107G>A
W02C12.3b.1:c.367-4107G>A
HGVSgCHROMOSOME_IV:g.4022689C>T
Sequence_detailsSMapS_parentSequenceW02C12
Flanking_sequencesTGTGCTGTGTTGCGAAAAATGGAAAACGGGGCGCAAATTTAGAAGGGATGTTGTGGAGAGATCGGAAATCAGAAATGAGT
Mapping_targetCHROMOSOME_IV
Source_location200CHROMOSOME_IV40226834022683
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023693
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00020930
TranscriptW02C12.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3e.1:c.187-4107G>A
Intron_number1/9
W02C12.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3d.1:c.187-4107G>A
Intron_number1/10
W02C12.3j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3j.1:c.214-4107G>A
Intron_number2/9
W02C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3b.1:c.367-4107G>A
Intron_number3/11
W02C12.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3c.1:c.367-4107G>A
Intron_number3/12
W02C12.3i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3i.1:c.214-4107G>A
Intron_number2/10
W02C12.3d.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3d.2:c.187-4107G>A
Intron_number2/11
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose