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WormBase Tree Display for Variation: WBVar02049669

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Name Class

WBVar02049669NamePublic_nameWBVar02049669
Other_namecewivar00778843
H14E04.2b.1:c.1669-160_1669-159del
H14E04.2d.1:c.1294-160_1294-159del
H14E04.2c.1:c.1681-160_1681-159del
H14E04.2a.1:c.1660-160_1660-159del
HGVSgCHROMOSOME_III:g.2384342_2384343del
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesCCAACATGACTAGGCTGTGCCTATTTTTAGGTCTCACCACGAAAACTACAGTACCCCTGGGTTTTCGTGGCGGGACCTAACATTGTTCAA
Mapping_targetH14E04
Source_location225CHROMOSOME_III23843322384333From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022886From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.1660-160_1660-159del
Intron_number10/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.1681-160_1681-159del
Intron_number11/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.1669-160_1669-159del
Intron_number10/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.1294-160_1294-159del
Intron_number7/8
MethodWGS_Flibotte