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WormBase Tree Display for Variation: WBVar01463220

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Name Class

WBVar01463220EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01463220
Other_nameC01G10.11a.1:c.86+781T>C
C01G10.11f.1:c.86+781T>C
C01G10.11b.1:c.86+781T>C
HGVSgCHROMOSOME_V:g.15072750T>C
Sequence_detailsSMapS_parentSequenceC01G10
Flanking_sequencesCAAGAAAAATTCGCAGAAATTTTCTTTTAGGCTTCCCTAAGTGTTTCTGACATACGTTCG
Mapping_targetC01G10
Type_of_mutationSubstitutiontc
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00005299From_analysisWGS_Andersen
WBStrain00005300From_analysisWGS_Andersen
WBStrain00005307From_analysisWGS_Andersen
WBStrain00005310From_analysisWGS_Andersen
WBStrain00030546From_analysisWGS_Andersen
WBStrain00030851From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193348876
dbSNP_ssss295524795
StatusLive
AffectsGeneWBGene00006808
WBGene00305285
TranscriptC01G10.11f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G10.11f.1:c.86+781T>C
Intron_number2/11
C01G10.11b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G10.11b.1:c.86+781T>C
Intron_number2/9
C01G10.11a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G10.11a.1:c.86+781T>C
Intron_number2/10
C25D7.19
ReferenceWBPaper00040707
MethodWGS_Andersen