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: WBVar02020388

expand all nodes | collapse all nodes | view schema

Name Class

WBVar02020388NamePublic_nameWBVar02020388
Other_namecewivar00748896
Y37E11C.1c.1:c.89+524_89+525insT
Y37E11C.1b.1:c.557+524_557+525insT
Y37E11C.1a.1:c.1082+524_1082+525insT
HGVSgCHROMOSOME_IV:g.3520296_3520297insT
Sequence_detailsSMapS_parentSequenceM57
Flanking_sequencesAAATACGTTTTTTTTTCTCGGAATTTAAAATTTTTATAGATTTTTACTTTTTTAAGCTAA
Mapping_targetM57
Source_location225CHROMOSOME_IV35202933520294From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006769
TranscriptY37E11C.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1c.1:c.89+524_89+525insT
Intron_number1/3
Y37E11C.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1b.1:c.557+524_557+525insT
Intron_number3/5
Y37E11C.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1a.1:c.1082+524_1082+525insT
Intron_number7/10
MethodWGS_Flibotte