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WormBase Tree Display for Variation: WBVar01561063

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Name Class

WBVar01561063NamePublic_nameWBVar01561063
Other_namecewivar00141638
F29C12.3a.1:c.2480+857A>T
F29C12.1a.1:c.1214T>A
CE19820:p.Leu405Gln
F29C12.3c.1:c.50+857A>T
CE37902:p.Leu403Gln
F29C12.3b.1:c.2486+857A>T
F29C12.1b.1:c.1208T>A
HGVSgCHROMOSOME_II:g.13109330T>A
Sequence_detailsSMapS_parentSequenceF29C12
Flanking_sequencesAACAGCAGTACCAGAATCAGAACAACTATCGCCACAGCCGCAGCAACCACAACTCCCAGT
Mapping_targetF29C12
Source_location225CHROMOSOME_II1310926013109260From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004120
WBGene00009245
TranscriptF29C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF29C12.3b.1:c.2486+857A>T
Intron_number11/17
F29C12.1a.1 (12)
F29C12.1b.1 (12)
F29C12.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF29C12.3c.1:c.50+857A>T
Intron_number1/6
F29C12.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF29C12.3a.1:c.2480+857A>T
Intron_number11/17
MethodWGS_Flibotte