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WormBase Tree Display for Variation: WBVar01758834

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Name Class

WBVar01758834NamePublic_nameWBVar01758834
Other_namecewivar00458538
C25A11.4f.1:c.456+383C>T
C25A11.4d.1:c.456+383C>T
C25A11.4a.1:c.-820+383C>T
C25A11.4c.1:c.456+383C>T
C25A11.4b.1:c.456+383C>T
HGVSgCHROMOSOME_X:g.9089092C>T
Sequence_detailsSMapS_parentSequenceH08J11
Flanking_sequencesATTTTATCATTGAAGACTGAATCCAGGTTCTGCATTTCTGATTATTTTTCCAAATTAACG
Mapping_targetH08J11
Source_location225CHROMOSOME_X90890369089036From_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
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000100
TranscriptC25A11.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4d.1:c.456+383C>T
Intron_number5/29
C25A11.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4a.1:c.-820+383C>T
Intron_number4/30
C25A11.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4f.1:c.456+383C>T
Intron_number4/28
C25A11.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4c.1:c.456+383C>T
Intron_number5/23
C25A11.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4b.1:c.456+383C>T
Intron_number4/18
MethodWGS_Flibotte