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WormBase Tree Display for Variation: WBVar02019057

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Name Class

WBVar02019057NamePublic_nameWBVar02019057
Other_namecewivar00747563
R10E12.1b.1:c.2164+102_2164+103insT
R10E12.1c.1:c.2164+102_2164+103insT
R10E12.1a.1:c.2164+102_2164+103insT
R10E12.1d.1:c.1076-660_1076-659insT
HGVSgCHROMOSOME_III:g.9960888_9960889insT
Sequence_detailsSMapS_parentSequenceR10E12
Flanking_sequencesTTTTCAGAAAAAAATTTAATGGGATTTTCATTTTTTCTTTTTTTTTCTCCCATTTTCTCA
Mapping_targetR10E12
Source_location225CHROMOSOME_III99608009960801From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00007010
TranscriptR10E12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR10E12.1d.1:c.1076-660_1076-659insT
Intron_number3/5
R10E12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR10E12.1c.1:c.2164+102_2164+103insT
Intron_number6/9
R10E12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR10E12.1b.1:c.2164+102_2164+103insT
Intron_number6/10
R10E12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR10E12.1a.1:c.2164+102_2164+103insT
Intron_number6/9
MethodWGS_Flibotte