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WormBase Tree Display for Variation: WBVar01255528

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Name Class

WBVar01255528EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01255528
Other_namecewivar00283789
T12B5.9:n.257A>C
T12B5.8.2:c.113+736A>C
T12B5.8.1:c.113+736A>C
HGVSgCHROMOSOME_III:g.942610T>G
Sequence_detailsSMapS_parentSequenceT12B5
Flanking_sequencesTCGCCATCACTCTTCTGTAGCCGAGCACGTGGAAGTGGTTTCTGATGGTGGGTTACTACATTGGAACTATGTTGCCAATTCACGTGTAGTTTCATCCGGC
Mapping_targetT12B5
Type_of_mutationSubstitutiontGPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539091919
StatusLive
AffectsGeneWBGene00023345
WBGene00020455
TranscriptT12B5.8.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT12B5.8.2:c.113+736A>C
Intron_number2/6
T12B5.8.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT12B5.8.1:c.113+736A>C
Intron_number2/5
PseudogeneT12B5.9VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScT12B5.9:n.257A>C
cDNA_position257
Exon_number2/7
ReferenceWBPaper00037807
MethodWGS_De_Bono