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WormBase Tree Display for Variation: WBVar01497659

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Name Class

WBVar01497659NamePublic_namegk961922
Other_nameT08A11.1e.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
T08A11.1b.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
T08A11.1c.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
T08A11.1h.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
T08A11.1f.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
T08A11.1d.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
T08A11.1g.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
T08A11.1a.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
HGVSgCHROMOSOME_III:g.4260671_4260724delinsAAAAATCGATTTTTGGTAGTT
Sequence_detailsSMapS_parentSequenceT08A11
Flanking_sequencesAATGGAAAAATCGATTTTTGGTAGTTTATGTATTAAATTTTGAGCAATGTTGCGTGAAAA
Mapping_targetT08A11
Source_location225CHROMOSOME_III42606444260697From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionAAAAATCGATTTTTGGTAGTT
Deletion
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00037992
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00011604
TranscriptT08A11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1e.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
Intron_number4/17
T08A11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1g.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
Intron_number5/18
T08A11.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1h.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
Intron_number5/18
T08A11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1d.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
Intron_number5/18
T08A11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1f.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
Intron_number4/17
T08A11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1c.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
Intron_number4/17
T08A11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1b.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
Intron_number5/18
T08A11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1a.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT
Intron_number5/18
ReferenceWBPaper00042537
MethodMillion_mutation