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WormBase Tree Display for Variation: WBVar01694015

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Name Class

WBVar01694015NamePublic_nameWBVar01694015
Other_namecewivar00390534
F53A3.4d.3:c.38+361C>T
F53A3.4b.1:c.4904+361C>T
F53A3.4a.1:c.4800-521C>T
F53A3.4d.1:c.38+361C>T
F53A3.4d.2:c.38+361C>T
HGVSgCHROMOSOME_III:g.1933663C>T
Sequence_detailsSMapS_parentSequenceF53A3
Flanking_sequencesATTTTCCCCCTAAAAATCGATATTTCCCCTGTGACTTGTGGTTTCTCAGATTTTTGGCATAAAAACTGTA
Mapping_targetF53A3
Source_location225CHROMOSOME_III19336541933654From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004128
TranscriptF53A3.4d.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A3.4d.2:c.38+361C>T
Intron_number6/10
F53A3.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A3.4d.1:c.38+361C>T
Intron_number7/11
F53A3.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A3.4b.1:c.4904+361C>T
Intron_number19/23
F53A3.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A3.4a.1:c.4800-521C>T
Intron_number19/23
F53A3.4d.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A3.4d.3:c.38+361C>T
Intron_number6/10
MethodWGS_Flibotte