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WormBase Tree Display for Variation: WBVar02035870

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Name Class

WBVar02035870NamePublic_nameWBVar02035870
Other_namecewivar00764536
T19D12.4a.1:c.3050-93_3050-70del
T19D12.12:n.31_54del
T19D12.11:n.1_24del
T19D12.4b.1:c.3011-93_3011-70del
HGVSgCHROMOSOME_II:g.6636854_6636877del
Sequence_detailsSMapS_parentSequenceT19D12
Flanking_sequencesTTTAAATTTAGTATGACAATACTGTCCAGAATATATATATATATATATATATATATAATC
Mapping_targetT19D12
Source_location225CHROMOSOME_II66368216636844From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023286From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00195800
WBGene00196647
WBGene00020579
TranscriptT19D12.11VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScT19D12.11:n.1_24del
cDNA_position1-24
Exon_number1/1
T19D12.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT19D12.4b.1:c.3011-93_3011-70del
Intron_number12/12
T19D12.12VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScT19D12.12:n.31_54del
cDNA_position31-54
Exon_number1/1
T19D12.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT19D12.4a.1:c.3050-93_3050-70del
Intron_number12/13
MethodWGS_Flibotte