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WormBase Tree Display for Variation: WBVar02115338

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Name Class

WBVar02115338NamePublic_nameWBVar02115338
Other_namecewivar00846056
K11D12.10c.1:c.1454+19_1455-22delinsGTAGTTTTTTTAAAA
K11D12.10d.1:c.1454+19_1455-22delinsGTAGTTTTTTTAAAA
K11D12.10b.1:c.1454+19_1455-22delinsGTAGTTTTTTTAAAA
K11D12.10a.1:c.1454+19_1455-22delinsGTAGTTTTTTTAAAA
HGVSgCHROMOSOME_V:g.5061180_5061194delinsTTTTAAAAAAACTAC
Sequence_detailsSMapS_parentSequenceY58A7A
Flanking_sequencesTCGAATTCCCTGAAATCGACAGTTATTATTTTTTTTTGTAAAACTAACTCTTTGGTCTTA
Mapping_targetY58A7A
Source_location225CHROMOSOME_V50611655061179From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionTTTTAAAAAAACTAC
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003374
TranscriptK11D12.10d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK11D12.10d.1:c.1454+19_1455-22delinsGTAGTTTTTTTAAAA
Intron_number9/15
K11D12.10b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK11D12.10b.1:c.1454+19_1455-22delinsGTAGTTTTTTTAAAA
Intron_number10/17
K11D12.10c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK11D12.10c.1:c.1454+19_1455-22delinsGTAGTTTTTTTAAAA
Intron_number10/18
K11D12.10a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK11D12.10a.1:c.1454+19_1455-22delinsGTAGTTTTTTTAAAA
Intron_number10/17
MethodWGS_Flibotte