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WormBase Tree Display for Variation: WBVar02061803

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Name Class

WBVar02061803NamePublic_nameWBVar02061803
Other_namecewivar00791041
M04G12.4b.1:c.1507-258_1507-257insGT
M04G12.4a.1:c.1594-258_1594-257insGT
M04G12.4d.1:c.1516-258_1516-257insGT
M04G12.4c.1:c.1603-258_1603-257insGT
HGVSgCHROMOSOME_V:g.13387052_13387053insAC
Sequence_detailsSMapS_parentSequenceM04G12
Flanking_sequencesTATCAACAAAACCTATAGTACAAAATTGATTAGTTAGTACTACTCGGCTACTAGTTTTTA
Mapping_targetM04G12
Source_location225CHROMOSOME_V1338703913387040From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionAC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00010868
TranscriptM04G12.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.4b.1:c.1507-258_1507-257insGT
Intron_number4/5
M04G12.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.4a.1:c.1594-258_1594-257insGT
Intron_number5/6
M04G12.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.4c.1:c.1603-258_1603-257insGT
Intron_number5/6
M04G12.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.4d.1:c.1516-258_1516-257insGT
Intron_number3/3
MethodWGS_Flibotte