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WormBase Tree Display for Variation: WBVar01945943

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Name Class

WBVar01945943NamePublic_nameWBVar01945943
Other_namecewivar00667468
T06H11.1d.1:c.442-649dup
T06H11.1c.1:c.298-649dup
T06H11.1e.1:c.217-649dup
T06H11.1b.1:c.412-649dup
T06H11.1g.1:c.286-649dup
T06H11.1a.1:c.526-649dup
T06H11.1f.1:c.562-649dup
HGVSgCHROMOSOME_X:g.10108441_10108442insT
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesAGAAAATAAACGTTCAAACAAGATTTTGACTTTTCACTATAACTCCTGTTCTATGTCACT
Mapping_targetT06H11
Source_location225CHROMOSOME_X1010838210108383From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionT
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.412-649dup
Intron_number4/12
T06H11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1g.1:c.286-649dup
Intron_number3/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.562-649dup
Intron_number5/14
T06H11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1e.1:c.217-649dup
Intron_number3/13
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.442-649dup
Intron_number2/11
T06H11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1a.1:c.526-649dup
Intron_number2/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.298-649dup
Intron_number3/13
MethodWGS_Flibotte