Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01888364

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01888364NamePublic_nameWBVar01888364
Other_namecewivar00603343
T06H11.1b.1:c.412-661G>A
T06H11.1a.1:c.526-661G>A
T06H11.1e.1:c.217-661G>A
T06H11.1d.1:c.442-661G>A
T06H11.1g.1:c.286-661G>A
T06H11.1f.1:c.562-661G>A
T06H11.1c.1:c.298-661G>A
HGVSgCHROMOSOME_X:g.10108454C>T
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesTTCAAACAAGATTTTGACTTTTCACTATAATCCTGTTCTATGTCACTCACAAAATAAGAT
Mapping_targetT06H11
Source_location225CHROMOSOME_X1010839510108395From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006792
TranscriptT06H11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1b.1:c.412-661G>A
Intron_number4/12
T06H11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1g.1:c.286-661G>A
Intron_number3/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.562-661G>A
Intron_number5/14
T06H11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1e.1:c.217-661G>A
Intron_number3/13
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.442-661G>A
Intron_number2/11
T06H11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1a.1:c.526-661G>A
Intron_number2/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.298-661G>A
Intron_number3/13
MethodWGS_Flibotte