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WormBase Tree Display for Variation: WBVar01946082

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Name Class

WBVar01946082NamePublic_nameWBVar01946082
Other_namecewivar00667607
F31B12.1k.1:c.1789+14_1790-51del
F31B12.1j.1:c.1618+14_1619-51del
F31B12.1i.1:c.1789+14_1790-51del
F31B12.1l.1:c.1618+14_1619-51del
F31B12.1d.1:c.1789+14_1790-51del
F31B12.1h.1:c.1618+14_1619-51del
F31B12.1g.1:c.1618+14_1619-51del
HGVSgCHROMOSOME_X:g.10825030_10825083del
Sequence_detailsSMapS_parentSequenceF31B12
Flanking_sequencesAAAAAACTTGAAGCTTCGTCTCGGTGTTTCATAAAAAACATACATGGAGTTGGTGGTTCG
Mapping_targetF31B12
Source_location225CHROMOSOME_X1082496510825018From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004036
TranscriptF31B12.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1j.1:c.1618+14_1619-51del
Intron_number15/63
F31B12.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1g.1:c.1618+14_1619-51del
Intron_number15/63
F31B12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1d.1:c.1789+14_1790-51del
Intron_number16/64
F31B12.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1h.1:c.1618+14_1619-51del
Intron_number15/63
F31B12.1l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1l.1:c.1618+14_1619-51del
Intron_number15/63
F31B12.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1i.1:c.1789+14_1790-51del
Intron_number16/64
F31B12.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1k.1:c.1789+14_1790-51del
Intron_number16/64
MethodWGS_Flibotte