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WormBase Tree Display for Variation: WBVar01551626

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Name Class

WBVar01551626NamePublic_nameWBVar01551626
Other_namecewivar00128683
T06H11.1d.1:c.292+4716A>C
T06H11.1f.1:c.413-8659A>C
T06H11.1b.1:c.262+7029A>C
HGVSgCHROMOSOME_X:g.10117990T>G
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesTGATGAAAGAACGACGAAATATAAAAAATTAAAAATAATTGAGGTCACACATCAATTTGA
Mapping_targetT06H11
Source_location225CHROMOSOME_X1011793110117931From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
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.262+7029A>C
Intron_number3/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.413-8659A>C
Intron_number4/14
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.292+4716A>C
Intron_number1/11
MethodWGS_Flibotte