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WormBase Tree Display for Variation: WBVar01782066

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Name Class

WBVar01782066NamePublic_nameWBVar01782066
Other_namecewivar00482889
Y59A8B.10b.1:c.921+149T>A
Y59A8B.10a.1:c.1224+149T>A
Y59A8B.10c.1:c.168+149T>A
Y59A8B.10d.1:c.1236+149T>A
HGVSgCHROMOSOME_V:g.18071714A>T
Sequence_detailsSMapS_parentSequenceY59A8B
Flanking_sequencesTTTTGAATTTGGAAGTTTTTGACCAATTTTCAGTTAAAATTTTAAAATTTCCAGCTTTTC
Mapping_targetY59A8B
Source_location225CHROMOSOME_V1807168618071686From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023191From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00013347
TranscriptY59A8B.10a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.10a.1:c.1224+149T>A
Intron_number5/6
Y59A8B.10d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.10d.1:c.1236+149T>A
Intron_number6/7
Y59A8B.10c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.10c.1:c.168+149T>A
Intron_number1/1
Y59A8B.10b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.10b.1:c.921+149T>A
Intron_number3/3
MethodWGS_Flibotte