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WormBase Tree Display for Variation: WBVar02010253

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Name Class

WBVar02010253NamePublic_nameWBVar02010253
Other_namecewivar00738274
H14E04.2b.1:c.1177+268_1178-248del
H14E04.2d.1:c.802+268_803-248del
H14E04.2c.1:c.1189+268_1190-248del
H14E04.2a.1:c.1168+268_1169-248del
HGVSgCHROMOSOME_III:g.2382180_2382231del
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesACGTAGTATTTTAAATTTTCAAAAAAAAAACATCTCATCGAGACCTTCAAATTGACCCCC
Mapping_targetH14E04
Source_location225CHROMOSOME_III23821702382221From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.1168+268_1169-248del
Intron_number8/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.1189+268_1190-248del
Intron_number9/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.1177+268_1178-248del
Intron_number8/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.802+268_803-248del
Intron_number5/8
MethodWGS_Flibotte