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WormBase Tree Display for Variation: WBVar01852286

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Name Class

WBVar01852286NamePublic_nameWBVar01852286
Other_namecewivar00565356
T08A11.1h.1:c.2593+1065C>A
T08A11.1g.1:c.2587+1065C>A
T08A11.1b.1:c.2593+1065C>A
T08A11.1c.1:c.2587+1065C>A
T08A11.1a.1:c.2587+1065C>A
T08A11.1f.1:c.2593+1065C>A
T08A11.1d.1:c.2593+1065C>A
T08A11.1e.1:c.2587+1065C>A
HGVSgCHROMOSOME_III:g.4256646G>T
Sequence_detailsSMapS_parentSequenceT08A11
Flanking_sequencesATGTTATAGAAAAATGCAAAGTTTGTAGTTATCTAGTTTAGATGTTCTGAACACGATTTC
Mapping_targetT08A11
Source_location225CHROMOSOME_III42566194256619From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00011604
TranscriptT08A11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1e.1:c.2587+1065C>A
Intron_number9/17
T08A11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1g.1:c.2587+1065C>A
Intron_number10/18
T08A11.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1h.1:c.2593+1065C>A
Intron_number10/18
T08A11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1d.1:c.2593+1065C>A
Intron_number10/18
T08A11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1f.1:c.2593+1065C>A
Intron_number9/17
T08A11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1c.1:c.2587+1065C>A
Intron_number9/17
T08A11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1b.1:c.2593+1065C>A
Intron_number10/18
T08A11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1a.1:c.2587+1065C>A
Intron_number10/18
MethodWGS_Flibotte