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WormBase Tree Display for Variation: WBVar01911567

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Name Class

WBVar01911567NamePublic_nameWBVar01911567
Other_namecewivar00627592
B0041.2b.1:c.17-9A>C
B0041.2a.1:c.-110-9A>C
B0041.2e.1:c.17-9A>C
B0041.2d.1:c.17-9A>C
B0041.2f.1:c.17-9A>C
HGVSgCHROMOSOME_I:g.4653589A>C
Sequence_detailsSMapS_parentSequenceB0041
Flanking_sequencesTTTTCGCTCAATTAATTCTAAACAATAATTTTTTTCAGGCAATGATCCGAATTATCGGCG
Mapping_targetB0041
Source_location225CHROMOSOME_I46535904653590From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00015007
TranscriptB0041.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2e.1:c.17-9A>C
Intron_number2/10
B0041.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2f.1:c.17-9A>C
Intron_number2/10
B0041.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2d.1:c.17-9A>C
Intron_number1/8
B0041.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2a.1:c.-110-9A>C
Intron_number1/10
B0041.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2b.1:c.17-9A>C
Intron_number2/10
MethodWGS_Flibotte