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WormBase Tree Display for Variation: WBVar01902373

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Name Class

WBVar01902373NamePublic_nameWBVar01902373
Other_namecewivar00617958
B0041.2a.2:c.1418-119C>T
B0041.2g.1:c.1358-119C>T
B0041.2c.1:c.1412-119C>T
B0041.2e.1:c.1484-119C>T
B0041.2d.1:c.1544-119C>T
B0041.2a.1:c.1418-119C>T
B0041.2b.1:c.1538-119C>T
B0041.2f.1:c.1478-119C>T
HGVSgCHROMOSOME_I:g.4657820C>T
Sequence_detailsSMapS_parentSequenceB0041
Flanking_sequencesCTGTAAAATCGCGCGTAGTCCACCGGAAATGACATGAGATCTCATGTCGATTTACAGTGG
Mapping_targetB0041
Source_location225CHROMOSOME_I46578214657821From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00015007
TranscriptB0041.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2f.1:c.1478-119C>T
Intron_number7/10
B0041.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2d.1:c.1544-119C>T
Intron_number6/8
B0041.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2c.1:c.1412-119C>T
Intron_number5/8
B0041.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2e.1:c.1484-119C>T
Intron_number7/10
B0041.2a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2a.2:c.1418-119C>T
Intron_number5/8
B0041.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2a.1:c.1418-119C>T
Intron_number7/10
B0041.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2g.1:c.1358-119C>T
Intron_number5/8
B0041.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2b.1:c.1538-119C>T
Intron_number7/10
MethodWGS_Flibotte