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WormBase Tree Display for Variation: WBVar01328429

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Name Class

WBVar01328429EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01328429
Other_namecewivar00149232
H19M22.2d.1:c.1615+25A>T
H19M22.2a.1:c.1615+25A>T
H19M22.2b.1:c.1615+25A>T
HGVSgCHROMOSOME_III:g.2661239A>T
Sequence_detailsSMapS_parentSequenceH19M22
Flanking_sequencesAGCAGTCGCAGGAAGTGTCAGATCAGGTATTACTTTTTGAACATTTTTTTAATGTATTAACAATTGAGTAAAGTAAACCCTAACCTTGTTCTTATATATG
Mapping_targetH19M22
Type_of_mutationSubstitutionaTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539183866
StatusLive
AffectsGeneWBGene00002915
TranscriptH19M22.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH19M22.2a.1:c.1615+25A>T
Intron_number6/26
H19M22.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH19M22.2d.1:c.1615+25A>T
Intron_number5/13
H19M22.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH19M22.2b.1:c.1615+25A>T
Intron_number6/28
ReferenceWBPaper00037807
MethodWGS_De_Bono