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WormBase Tree Display for Variation: WBVar01645028

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Name Class

WBVar01645028NamePublic_nameWBVar01645028
Other_namecewivar00331347
F47D12.1e.1:c.65+20A>G
F47D12.1c.1:c.905+20A>G
F47D12.1a.1:c.905+20A>G
F47D12.1b.1:c.905+20A>G
HGVSgCHROMOSOME_III:g.6317902A>G
Sequence_detailsSMapS_parentSequenceF47D12
Flanking_sequencesAACACTTACAGGTGGGTTCAAGAAGTGAAGCTTGTTCTGAAAGTGATTAAAAAATTACAA
Mapping_targetF47D12
Source_location225CHROMOSOME_III63178506317850From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001518
TranscriptF47D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1b.1:c.905+20A>G
Intron_number7/12
F47D12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1e.1:c.65+20A>G
Intron_number2/7
F47D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1a.1:c.905+20A>G
Intron_number7/13
F47D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1c.1:c.905+20A>G
Intron_number7/12
MethodWGS_Flibotte