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WormBase Tree Display for Variation: WBVar02126501

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Name Class

WBVar02126501EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh5495
Other_nameY37E3.11i.1:c.787-112C>T
Y37E3.11e.1:c.205-112C>T
Y37E3.11a.1:c.724-112C>T
Y37E3.11d.1:c.520-112C>T
Y37E3.11b.1:c.745-112C>T
Y37E3.11c.1:c.583-112C>T
HGVSgCHROMOSOME_I:g.2084227C>T
Sequence_detailsSMapS_parentSequenceY37E3
Flanking_sequencesTTAAATATAAAATCAGGGGAAATTTTTTTGATTAGATATTGGAATCAGGGGAAAATTTGGAGTCGATTAAAAATATTTCC
Mapping_targetCHROMOSOME_I
Source_location200CHROMOSOME_I20842292084229
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023667
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00021352
TranscriptY37E3.11i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E3.11i.1:c.787-112C>T
Intron_number8/11
Y37E3.11e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E3.11e.1:c.205-112C>T
Intron_number1/3
Y37E3.11a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E3.11a.1:c.724-112C>T
Intron_number6/9
Y37E3.11d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E3.11d.1:c.520-112C>T
Intron_number3/5
Y37E3.11b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E3.11b.1:c.745-112C>T
Intron_number7/10
Y37E3.11c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E3.11c.1:c.583-112C>T
Intron_number5/7
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose