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WormBase Tree Display for Variation: WBVar01766481

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Name Class

WBVar01766481NamePublic_nameWBVar01766481
Other_namecewivar00466617
T27D12.2e.1:c.186-524A>G
T27D12.2a.1:c.186-524A>G
T27D12.2d.1:c.201-524A>G
T27D12.2c.1:c.387-524A>G
T27D12.2b.1:c.186-524A>G
HGVSgCHROMOSOME_II:g.11851835T>C
Sequence_detailsSMapS_parentSequenceT27D12
Flanking_sequencesATCTGATCACTGAGAACCGTGATGATGAAAAGTGTGGTAGAGGAAGTGGCGGAGGAAATT
Mapping_targetT27D12
Source_location225CHROMOSOME_II1185177211851772From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000528
TranscriptT27D12.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27D12.2b.1:c.186-524A>G
Intron_number3/18
T27D12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27D12.2a.1:c.186-524A>G
Intron_number3/18
T27D12.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27D12.2c.1:c.387-524A>G
Intron_number3/17
T27D12.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27D12.2d.1:c.201-524A>G
Intron_number1/15
T27D12.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27D12.2e.1:c.186-524A>G
Intron_number3/19
MethodWGS_Flibotte