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WormBase Tree Display for Variation: WBVar01681895

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Name Class

WBVar01681895NamePublic_nameWBVar01681895
Other_namecewivar00372483
K01A2.8d.1:c.324-119G>C
K01A2.8c.1:c.177-119G>C
K01A2.8c.3:c.177-119G>C
K01A2.8c.2:c.177-119G>C
K01A2.4a.2:c.*95+344C>G
K01A2.8a.1:c.309-119G>C
HGVSgCHROMOSOME_II:g.309888C>G
Sequence_detailsSMapS_parentSequenceK01A2
Flanking_sequencesCATAATAAAACACTTCAAAAATTTTCAAAAGTTTTTTTGGAAAGGTTTTTTTTTGAAATT
Mapping_targetK01A2
Source_location225CHROMOSOME_II309888309888From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019279
WBGene00019282
TranscriptK01A2.8d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8d.1:c.324-119G>C
Intron_number3/4
K01A2.8c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.1:c.177-119G>C
Intron_number3/5
K01A2.8a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8a.1:c.309-119G>C
Intron_number4/6
K01A2.8c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.2:c.177-119G>C
Intron_number4/6
K01A2.8c.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.3:c.177-119G>C
Intron_number4/6
K01A2.4a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.4a.2:c.*95+344C>G
Intron_number12/12
MethodWGS_Flibotte