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WormBase Tree Display for Variation: WBVar01727831

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Name Class

WBVar01727831NamePublic_nameWBVar01727831
Other_namecewivar00426304
C11D2.6m.1:c.33+1302G>A
C11D2.6o.1:c.33+1302G>A
C11D2.99:n.229C>T
C11D2.6p.1:c.33+1302G>A
C11D2.6n.1:c.33+1302G>A
HGVSgCHROMOSOME_IV:g.6182523C>T
Sequence_detailsSMapS_parentSequenceC11D2
Flanking_sequencesATTTGTCACCCTCTTTTCATATATTGGCATCGATGGAAAGGGTCCAATCGGTTGGACAAG
Mapping_targetC11D2
Source_location225CHROMOSOME_IV61825126182512From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00196792
WBGene00006809
TranscriptC11D2.6o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6o.1:c.33+1302G>A
Intron_number1/28
C11D2.6p.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6p.1:c.33+1302G>A
Intron_number1/28
C11D2.6n.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6n.1:c.33+1302G>A
Intron_number1/27
C11D2.99VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScC11D2.99:n.229C>T
cDNA_position229
Exon_number1/1
C11D2.6m.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6m.1:c.33+1302G>A
Intron_number1/29
MethodWGS_Flibotte