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WormBase Tree Display for Variation: WBVar01551603

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Name Class

WBVar01551603NamePublic_nameWBVar01551603
Other_namecewivar00128660
T06H11.1g.1:c.136+1886G>T
T06H11.1f.1:c.413-2455G>T
T06H11.1d.1:c.293-2455G>T
T06H11.1b.1:c.263-2455G>T
T06H11.1c.1:c.149-2455G>T
HGVSgCHROMOSOME_X:g.10111786C>A
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesCTAATTCAAACTTTTTTGTTTTTTCTGCTGAAAATTCAAATTACTTTGTAGATTGGTTTT
Mapping_targetT06H11
Source_location225CHROMOSOME_X1011172710111727From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCA
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.263-2455G>T
Intron_number3/12
T06H11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1g.1:c.136+1886G>T
Intron_number2/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.413-2455G>T
Intron_number4/14
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.293-2455G>T
Intron_number1/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.149-2455G>T
Intron_number2/13
MethodWGS_Flibotte