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WormBase Tree Display for Variation: WBVar01527599

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Name Class

WBVar01527599NamePublic_nameWBVar01527599
Other_namecewivar00060834
T06H11.1e.1:c.67+299G>C
T06H11.1d.1:c.293-1442G>C
T06H11.1c.1:c.149-1442G>C
T06H11.1b.1:c.263-1442G>C
T06H11.1g.1:c.137-1442G>C
T06H11.1f.1:c.413-1442G>C
HGVSgCHROMOSOME_X:g.10110773C>G
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesACCGTAACCCTATTGTACCACTACAGTACCCCGACTATATCCTACACTAAGCCCAACTCACATTCCCTCC
Mapping_targetT06H11
Source_location225CHROMOSOME_X1011071410110714From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (18)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006792
TranscriptT06H11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1b.1:c.263-1442G>C
Intron_number3/12
T06H11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1g.1:c.137-1442G>C
Intron_number2/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.413-1442G>C
Intron_number4/14
T06H11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1e.1:c.67+299G>C
Intron_number2/13
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.293-1442G>C
Intron_number1/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.149-1442G>C
Intron_number2/13
MethodWGS_Flibotte