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WormBase Tree Display for Variation: WBVar01567391

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Name Class

WBVar01567391NamePublic_nameWBVar01567391
Other_namecewivar00151906
T21C12.1o.1:c.212-218T>A
T21C12.1e.1:c.*153-218T>A
T21C12.1f.1:c.716-218T>A
T21C12.1d.1:c.*153-218T>A
T21C12.1h.1:c.164-218T>A
T21C12.1c.1:c.*153-218T>A
HGVSgCHROMOSOME_III:g.10531011T>A
Sequence_detailsSMapS_parentSequenceT21C12
Flanking_sequencesCCGACAATAACATTTGGCCATTGATTTTTTACTGAGAAAGTCATAAATCGAAATTTTAAA
Mapping_targetT21C12
Source_location225CHROMOSOME_III1053091310530913From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006784
TranscriptT21C12.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1h.1:c.164-218T>A
Intron_number2/6
T21C12.1o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1o.1:c.212-218T>A
Intron_number2/5
T21C12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1d.1:c.*153-218T>A
Intron_number14/17
T21C12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.1:c.*153-218T>A
Intron_number15/18
T21C12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1e.1:c.*153-218T>A
Intron_number16/19
T21C12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1f.1:c.716-218T>A
Intron_number7/11
MethodWGS_Flibotte