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WormBase Tree Display for Variation: WBVar01571026

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Name Class

WBVar01571026NamePublic_nameWBVar01571026
Other_namecewivar00157299
C34E11.2g.1:c.95+47C>T
C34E11.2f.1:c.95+47C>T
C34E11.2d.1:c.95+47C>T
C34E11.2e.1:c.95+47C>T
C34E11.2a.1:c.95+47C>T
HGVSgCHROMOSOME_X:g.11814512G>A
Sequence_detailsSMapS_parentSequenceC34E11
Flanking_sequencesACCCCACCCAGAGAGAAAAAAATTGAAGACATAAATAGGAACACACAGGAAGCATGAAAA
Mapping_targetC34E11
Source_location225CHROMOSOME_X1181444411814444From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00007935
TranscriptC34E11.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2g.1:c.95+47C>T
Intron_number1/12
C34E11.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2a.1:c.95+47C>T
Intron_number1/15
C34E11.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2f.1:c.95+47C>T
Intron_number2/15
C34E11.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2e.1:c.95+47C>T
Intron_number1/15
C34E11.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2d.1:c.95+47C>T
Intron_number1/14
MethodWGS_Flibotte