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WormBase Tree Display for Variation: WBVar01616299

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Name Class

WBVar01616299NamePublic_nameWBVar01616299
Other_namecewivar00295786
T27C4.4d.1:c.*885-471T>G
T27C4.4b.2:c.2608-471T>G
T27C4.4b.1:c.2608-471T>G
T27C4.4e.1:c.2203-471T>G
T27C4.4a.1:c.2919-471T>G
HGVSgCHROMOSOME_V:g.3711882T>G
Sequence_detailsSMapS_parentSequenceT27C4
Flanking_sequencesGTATCTACAGTAACCCTACAGTAGTTAAAGATCTACAGTAACTTTGAAAGCTTATCAAAC
Mapping_targetT27C4
Source_location225CHROMOSOME_V37118693711869From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003025
TranscriptT27C4.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4d.1:c.*885-471T>G
Intron_number8/8
T27C4.4b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4b.2:c.2608-471T>G
Intron_number7/8
T27C4.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4a.1:c.2919-471T>G
Intron_number8/9
T27C4.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4e.1:c.2203-471T>G
Intron_number4/4
T27C4.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4b.1:c.2608-471T>G
Intron_number7/8
MethodWGS_Flibotte