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WormBase Tree Display for Variation: WBVar01551635

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Name Class

WBVar01551635NamePublic_nameWBVar01551635
Other_namecewivar00128692
T06H11.1d.1:c.292+707A>T
T06H11.1f.1:c.412+6930A>T
T06H11.1b.1:c.262+3020A>T
HGVSgCHROMOSOME_X:g.10121999T>A
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesGACCATCATGTCTCTTATTATCAAAAAAAAACAATAGAATGTCAGATCAAAAATTAAATA
Mapping_targetT06H11
Source_location225CHROMOSOME_X1012194010121940From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006792
TranscriptT06H11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1b.1:c.262+3020A>T
Intron_number3/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.412+6930A>T
Intron_number4/14
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.292+707A>T
Intron_number1/11
MethodWGS_Flibotte