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WormBase Tree Display for Variation: WBVar01514866

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Name Class

WBVar01514866NamePublic_nameWBVar01514866
Other_namecewivar00037705
Y37E11C.1c.1:c.90-1557G>A
Y37E11C.1a.1:c.1083-1557G>A
Y37E11C.1b.1:c.558-1557G>A
HGVSgCHROMOSOME_IV:g.3521410G>A
Sequence_detailsSMapS_parentSequenceM57
Flanking_sequencesCATTGGCCCTGGAAATGAGCAAATCTGGGTTCAAATTAACGACAAAACCCTACTTTTTAA
Mapping_targetM57
Source_location225CHROMOSOME_IV35214073521407From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000032From_analysisMillion_mutation_project_reanalysis
WBStrain00022883From_analysisMillion_mutation_project_reanalysis
WBStrain00022887From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006769
TranscriptY37E11C.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1c.1:c.90-1557G>A
Intron_number1/3
Y37E11C.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1b.1:c.558-1557G>A
Intron_number3/5
Y37E11C.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1a.1:c.1083-1557G>A
Intron_number7/10
MethodWGS_Flibotte