Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01566653

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01566653NamePublic_nameWBVar01566653
Other_namecewivar00150670
F47D12.1b.1:c.734+940A>G
F47D12.1a.1:c.734+940A>G
F47D12.1c.1:c.734+940A>G
HGVSgCHROMOSOME_III:g.6316359A>G
Sequence_detailsSMapS_parentSequenceF47D12
Flanking_sequencesATAGGTCTACAAGGTAGAAGTAAATCACCTCATCTTCTTTTTTCTGACTTTCCAATGTTA
Mapping_targetF47D12
Source_location225CHROMOSOME_III63163076316307From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001518
TranscriptF47D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1b.1:c.734+940A>G
Intron_number6/12
F47D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1a.1:c.734+940A>G
Intron_number6/13
F47D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1c.1:c.734+940A>G
Intron_number6/12
MethodWGS_Flibotte