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WormBase Tree Display for Variation: WBVar01966138

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Name Class

WBVar01966138NamePublic_nameWBVar01966138
Other_namecewivar00692094
W02C12.3f.1:c.*907del
W02C12.3d.1:c.*907del
W02C12.3a.1:c.*907del
W02C12.3b.1:c.*907del
W02C12.3c.1:c.*907del
W02C12.3h.2:c.*907del
W02C12.3a.2:c.*907del
W02C12.3g.1:c.*1155del
W02C12.3d.2:c.*907del
HGVSgCHROMOSOME_IV:g.4014852del
Sequence_detailsSMapS_parentSequenceW02C12
Flanking_sequencesCGCAATAGGAAAATAATGAAAAAAACAATGTTTTTGTTGGGTGTTTTTGGAATCATTGTC
Mapping_targetW02C12
Source_location225CHROMOSOME_IV40148464014846From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00020930
TranscriptW02C12.3d.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3d.1:c.*907del
cDNA_position2302
Exon_number11/11
W02C12.3g.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3g.1:c.*1155del
cDNA_position2531
Exon_number11/11
W02C12.3c.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3c.1:c.*907del
cDNA_position2523
Exon_number13/13
W02C12.3h.2VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3h.2:c.*907del
cDNA_position2096
Exon_number10/10
W02C12.3a.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3a.1:c.*907del
cDNA_position2465
Exon_number12/12
W02C12.3f.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3f.1:c.*907del
cDNA_position2392
Exon_number11/11
W02C12.3a.2VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3a.2:c.*907del
cDNA_position2462
Exon_number12/12
W02C12.3b.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3b.1:c.*907del
cDNA_position2448
Exon_number12/12
W02C12.3d.2VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScW02C12.3d.2:c.*907del
cDNA_position2496
Exon_number12/12
MethodWGS_Flibotte