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WormBase Tree Display for Variation: WBVar01899766

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Name Class

WBVar01899766NamePublic_nameWBVar01899766
Other_namecewivar00615257
Y59A8B.22a.1:c.931+570T>C
Y59A8B.22b.1:c.640+570T>C
Y59A8B.22c.1:c.541+570T>C
HGVSgCHROMOSOME_V:g.17974167A>G
Sequence_detailsSMapS_parentSequenceY59A8B
Flanking_sequencesTTTAAAAACGTGCAAGCGCGCTCCATCGAACAAATCCAATTGGCGGTAATTCAAATAGGAATTAGGCAAAACTGAGATTTTTTCAATTTTCAAAAAATCATATAAAATTTATAATTTTCT
Mapping_targetY59A8B
Source_location225CHROMOSOME_V1797414117974141From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00013354
TranscriptY59A8B.22b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.22b.1:c.640+570T>C
Intron_number5/8
Y59A8B.22a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.22a.1:c.931+570T>C
Intron_number7/11
Y59A8B.22c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.22c.1:c.541+570T>C
Intron_number4/7
MethodWGS_Flibotte