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WormBase Tree Display for Variation: WBVar01540631

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Name Class

WBVar01540631NamePublic_nameWBVar01540631
Other_namecewivar00102727
BE0003N10.6d.1:c.168+481G>C
BE0003N10.6c.1:c.414+481G>C
BE0003N10.6b.1:c.489+481G>C
BE0003N10.6a.1:c.807+481G>C
HGVSgCHROMOSOME_III:g.1057249C>G
Sequence_detailsSMapS_parentSequenceBE0003N10
Flanking_sequencesGAAATTTTGCAAAAATCCACGTAGATTATTGATTTTTCATGAATTTTGCAAAAATCCACGTAGATTATTGATTTTTCATG
Mapping_targetBE0003N10
Source_location225CHROMOSOME_III10572391057239From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00255598
TranscriptBE0003N10.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScBE0003N10.6a.1:c.807+481G>C
Intron_number5/6
BE0003N10.6d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScBE0003N10.6d.1:c.168+481G>C
Intron_number1/1
BE0003N10.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScBE0003N10.6b.1:c.489+481G>C
Intron_number3/3
BE0003N10.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScBE0003N10.6c.1:c.414+481G>C
Intron_number2/2
MethodWGS_Flibotte