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WormBase Tree Display for Variation: WBVar02084809

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Name Class

WBVar02084809NamePublic_nameWBVar02084809
Other_namecewivar00814498
C52E12.2b.1:c.599+1941_599+1946delinsAAAAGAAAATTCAAAGGG
C52E12.2a.2:c.599+1941_599+1946delinsAAAAGAAAATTCAAAGGG
C52E12.2a.1:c.599+1941_599+1946delinsAAAAGAAAATTCAAAGGG
HGVSgCHROMOSOME_II:g.6999094_6999099delinsAAAAGAAAATTCAAAGGG
Sequence_detailsSMapS_parentSequenceC52E12
Flanking_sequencesTTGATTTTTTCGAAAAGAAAATTCAAAGGGCTTATGAAAAATTTTAAATTTTTTTTCGAA
Mapping_targetC52E12
Source_location225CHROMOSOME_II69990526999057From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionAAAAGAAAATTCAAAGGG
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006831
TranscriptC52E12.2a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC52E12.2a.2:c.599+1941_599+1946delinsAAAAGAAAATTCAAAGGG
Intron_number5/23
C52E12.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC52E12.2b.1:c.599+1941_599+1946delinsAAAAGAAAATTCAAAGGG
Intron_number5/24
C52E12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC52E12.2a.1:c.599+1941_599+1946delinsAAAAGAAAATTCAAAGGG
Intron_number5/23
MethodWGS_Flibotte