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WormBase Tree Display for Variation: WBVar01551605

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Name Class

WBVar01551605NamePublic_nameWBVar01551605
Other_namecewivar00128662
T06H11.1g.1:c.136+481T>A
T06H11.1d.1:c.293-3860T>A
T06H11.1f.1:c.413-3860T>A
T06H11.1c.1:c.149-3860T>A
T06H11.1b.1:c.263-3860T>A
HGVSgCHROMOSOME_X:g.10113191A>T
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesAAAATCCGAAAAAATTGAAAAATAGGAAAATTTTTTGAGCGTAGTTTTGAGGATCAATCA
Mapping_targetT06H11
Source_location225CHROMOSOME_X1011313210113132From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_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.263-3860T>A
Intron_number3/12
T06H11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1g.1:c.136+481T>A
Intron_number2/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.413-3860T>A
Intron_number4/14
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.293-3860T>A
Intron_number1/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.149-3860T>A
Intron_number2/13
MethodWGS_Flibotte