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WormBase Tree Display for Variation: WBVar01853904

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Name Class

WBVar01853904NamePublic_nameWBVar01853904
Other_name (11)
HGVSgCHROMOSOME_IV:g.8228770A>G
Sequence_detailsSMapS_parentSequenceT09A12
Flanking_sequencesAATTGTTTGGTTATGTGTACATCGACAATGAACAAAGTACATACCTTTGACTACTGTACA
Mapping_targetT09A12
Source_location225CHROMOSOME_IV82287568228756From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003656
TranscriptT09A12.4i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4i.1:c.298+15T>C
Intron_number3/7
T09A12.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4c.1:c.946+15T>C
Intron_number8/13
T09A12.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4b.1:c.325+15T>C
Intron_number4/9
T09A12.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4f.1:c.940+15T>C
Intron_number8/13
T09A12.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4a.1:c.478+15T>C
Intron_number4/9
T09A12.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4d.1:c.724+15T>C
Intron_number6/10
T09A12.4g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4g.1:c.718+15T>C
Intron_number6/10
T09A12.4j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4j.1:c.331+15T>C
Intron_number4/9
T09A12.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4e.1:c.304+15T>C
Intron_number3/7
T09A12.4h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4h.1:c.484+15T>C
Intron_number4/8
MethodWGS_Flibotte