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WormBase Tree Display for Variation: WBVar01946214

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Name Class

WBVar01946214NamePublic_nameWBVar01946214
Other_namecewivar00667739
T21H8.1p.1:c.73+49del
T21H8.1o.1:c.151+49del
T21H8.1i.1:c.73+49del
T21H8.1h.1:c.151+49del
T21H8.1g.1:c.151+49del
T21H8.1j.1:c.73+49del
T21H8.1k.1:c.-126+49del
HGVSgCHROMOSOME_X:g.13880893del
Sequence_detailsSMapS_parentSequenceT21H8
Flanking_sequencesAAACTCAGCGCCATGGTATAATTGTTTGGTAAAAAAAAACTCTAAAACTATTGCAGTTTT
Mapping_targetT21H8
Source_location225CHROMOSOME_X1388082513880825From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (14)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00011904
TranscriptT21H8.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21H8.1h.1:c.151+49del
Intron_number2/17
T21H8.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21H8.1i.1:c.73+49del
Intron_number2/17
T21H8.1p.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21H8.1p.1:c.73+49del
Intron_number1/3
T21H8.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21H8.1j.1:c.73+49del
Intron_number1/16
T21H8.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21H8.1g.1:c.151+49del
Intron_number3/18
T21H8.1o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21H8.1o.1:c.151+49del
Intron_number2/5
T21H8.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21H8.1k.1:c.-126+49del
Intron_number1/16
MethodWGS_Flibotte