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WormBase Tree Display for Variation: WBVar01681896

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Name Class

WBVar01681896NamePublic_nameWBVar01681896
Other_namecewivar00372484
K01A2.8d.1:c.323+129G>A
K01A2.8c.2:c.176+129G>A
K01A2.8a.1:c.308+129G>A
K01A2.8c.1:c.176+129G>A
K01A2.4a.2:c.*95+489C>T
K01A2.8c.3:c.176+129G>A
HGVSgCHROMOSOME_II:g.310033C>T
Sequence_detailsSMapS_parentSequenceK01A2
Flanking_sequencesGCCAAAACAATTGTCTTAATTTTAAAAAGTTGTACCGACAATATCAAAATTGGTATTAAA
Mapping_targetK01A2
Source_location225CHROMOSOME_II310033310033From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019279
WBGene00019282
TranscriptK01A2.8d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8d.1:c.323+129G>A
Intron_number3/4
K01A2.8c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.1:c.176+129G>A
Intron_number3/5
K01A2.8a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8a.1:c.308+129G>A
Intron_number4/6
K01A2.8c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.2:c.176+129G>A
Intron_number4/6
K01A2.8c.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.3:c.176+129G>A
Intron_number4/6
K01A2.4a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.4a.2:c.*95+489C>T
Intron_number12/12
MethodWGS_Flibotte