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WormBase Tree Display for Variation: WBVar01938002

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Name Class

WBVar01938002NamePublic_nameWBVar01938002
Other_namecewivar00658519
H14E04.2a.1:c.1497+27_1497+28del
H14E04.2c.1:c.1518+27_1518+28del
H14E04.2b.1:c.1506+27_1506+28del
H14E04.2d.1:c.1131+27_1131+28del
HGVSgCHROMOSOME_III:g.2382834_2382835del
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesTAAGGTTTCTGGAGAAACACGAAGAAAATTAAAAAAAAAAACGGAGAAATTTGAGCCAAA
Mapping_targetH14E04
Source_location225CHROMOSOME_III23828242382825From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.1497+27_1497+28del
Intron_number9/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.1518+27_1518+28del
Intron_number10/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.1506+27_1506+28del
Intron_number9/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.1131+27_1131+28del
Intron_number6/8
MethodWGS_Flibotte