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WormBase Tree Display for Variation: WBVar01995639

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Name Class

WBVar01995639NamePublic_nameWBVar01995639
Other_name (11)
HGVSgCHROMOSOME_III:g.9554870del
Sequence_detailsSMapS_parentSequenceZK1098
Flanking_sequencesGGTTCTATACATTTTGTGCAAAAAATTGAGAAAAATTTTAAGCTCAAGACGTAAGTACTA
Mapping_targetZK1098
Source_location225CHROMOSOME_III95547859554785From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006755
TranscriptZK1098.10g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10g.1:c.1681+34del
Intron_number10/13
ZK1098.10b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10b.1:c.2632+34del
Intron_number17/21
ZK1098.10a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10a.2:c.2578+34del
Intron_number18/22
ZK1098.10o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10o.1:c.1699+34del
Intron_number11/14
ZK1098.10a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10a.1:c.2578+34del
Intron_number19/23
ZK1098.10f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10f.1:c.1885+34del
Intron_number12/15
ZK1098.10e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10e.1:c.2731+34del
Intron_number18/22
ZK1098.10p.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10p.1:c.883+34del
Intron_number7/10
ZK1098.10c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10c.1:c.799+34del
Intron_number6/9
ZK1098.10d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScZK1098.10d.1:c.2716+34del
Intron_number18/22
MethodWGS_Flibotte