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WormBase Tree Display for Variation: WBVar02095412

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Name Class

WBVar02095412NamePublic_nameWBVar02095412
Other_namecewivar00825442
B0041.2a.2:c.1135+87_1135+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
B0041.2c.1:c.1135+87_1135+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
B0041.2f.1:c.1261+87_1261+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
B0041.2a.1:c.1135+87_1135+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
B0041.2e.1:c.1261+87_1261+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
B0041.2b.1:c.1261+87_1261+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
B0041.2d.1:c.1261+87_1261+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
B0041.2g.1:c.1135+87_1135+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
HGVSgCHROMOSOME_I:g.4656867_4656892delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Sequence_detailsSMapS_parentSequenceB0041
Flanking_sequencesTTCGTTTAAAATTAATTATACCAATTTTTTTTTTTTTACATCGAAATTGATGATAAAATT
Mapping_targetB0041
Source_location225CHROMOSOME_I46568684656893From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionGTTGCGTTTTCCGTTTTTTTAAATAT
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00015007
TranscriptB0041.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2f.1:c.1261+87_1261+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Intron_number6/10
B0041.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2d.1:c.1261+87_1261+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Intron_number5/8
B0041.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2c.1:c.1135+87_1135+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Intron_number4/8
B0041.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2e.1:c.1261+87_1261+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Intron_number6/10
B0041.2a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2a.2:c.1135+87_1135+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Intron_number4/8
B0041.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2a.1:c.1135+87_1135+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Intron_number6/10
B0041.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2g.1:c.1135+87_1135+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Intron_number4/8
B0041.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2b.1:c.1261+87_1261+112delinsGTTGCGTTTTCCGTTTTTTTAAATAT
Intron_number6/10
MethodWGS_Flibotte