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WormBase Tree Display for Variation: WBVar01654600

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Name Class

WBVar01654600NamePublic_nameWBVar01654600
Other_namecewivar00341690
Y59A8B.13c.1:c.482+28C>T
Y59A8B.13b.1:c.482+28C>T
Y59A8B.13a.1:c.482+28C>T
Y59A8B.13d.1:c.482+28C>T
HGVSgCHROMOSOME_V:g.18089003C>T
Sequence_detailsSMapS_parentSequenceY59A8B
Flanking_sequencesTAGGTTCGCGTAAAAATTCGATTTTTTCCACCAAAAATCGAAAAAATCGAGTTTTCCGTC
Mapping_targetY59A8B
Source_location225CHROMOSOME_V1808897518088975From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00013350
TranscriptY59A8B.13b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.13b.1:c.482+28C>T
Intron_number6/10
Y59A8B.13c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.13c.1:c.482+28C>T
Intron_number5/8
Y59A8B.13a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.13a.1:c.482+28C>T
Intron_number5/8
Y59A8B.13d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.13d.1:c.482+28C>T
Intron_number6/10
MethodWGS_Flibotte