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: WBVar02081741

expand all nodes | collapse all nodes | view schema

Name Class

WBVar02081741NamePublic_nameWBVar02081741
Other_namecewivar00811353
Y41C4A.4b.1:c.150-491_150-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Y41C4A.4c.1:c.117-491_117-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Y41C4A.4a.1:c.150-491_150-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Y41C4A.4g.1:c.468-491_468-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Y41C4A.4d.1:c.168-491_168-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Y41C4A.4e.1:c.93-491_93-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
HGVSgCHROMOSOME_III:g.11684719_11684720insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Sequence_detailsSMapS_parentSequenceY41C4A
Flanking_sequencesTTGTGGAAAATCGGCACATTGCCGGAATTTAAATTTGTGGAAAATCGGCAAATTGCCGGC
Mapping_targetY41C4A
Source_location225CHROMOSOME_III1168461911684620From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (17)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000793
TranscriptY41C4A.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4e.1:c.93-491_93-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Intron_number3/8
Y41C4A.4g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4g.1:c.468-491_468-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Intron_number1/6
Y41C4A.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4b.1:c.150-491_150-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Intron_number2/6
Y41C4A.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4a.1:c.150-491_150-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Intron_number3/8
Y41C4A.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4d.1:c.168-491_168-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Intron_number3/8
Y41C4A.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4c.1:c.117-491_117-490insTGTGAATTGAAATTTGTGGAAAATCGGCAAATTG
Intron_number2/6
MethodWGS_Flibotte