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WormBase Tree Display for Variation: WBVar01939766

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Name Class

WBVar01939766NamePublic_nameWBVar01939766
Other_namecewivar00660642
T21C12.1k.1:c.238-17del
T21C12.1d.1:c.238-17del
T21C12.1f.1:c.238-17del
T21C12.1b.1:c.238-17del
T21C12.1j.1:c.238-17del
T21C12.1c.1:c.238-17del
T21C12.1e.1:c.238-17del
T21C12.1c.2:c.238-17del
HGVSgCHROMOSOME_III:g.10522899del
Sequence_detailsSMapS_parentSequenceT21C12
Flanking_sequencesGTGGGAGGACTGCACCATCTAATTTAACTCTTTTTTTTCATTCCAGGACTTCACATTAGA
Mapping_targetT21C12
Source_location225CHROMOSOME_III1052280110522801From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006784
TranscriptT21C12.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1k.1:c.238-17del
Intron_number3/11
T21C12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.1:c.238-17del
Intron_number4/18
T21C12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1e.1:c.238-17del
Intron_number4/19
T21C12.1c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.2:c.238-17del
Intron_number4/14
T21C12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1b.1:c.238-17del
Intron_number4/14
T21C12.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1j.1:c.238-17del
Intron_number3/5
T21C12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1d.1:c.238-17del
Intron_number4/17
T21C12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1f.1:c.238-17del
Intron_number4/11
MethodWGS_Flibotte