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WormBase Tree Display for Variation: WBVar01826386

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Name Class

WBVar01826386NamePublic_nameWBVar01826386
Other_name (11)
HGVSgCHROMOSOME_I:g.4080128T>A
Sequence_detailsSMapS_parentSequenceC24G7
Flanking_sequencesCCAATAATTTTTTTTTAATTCTGGCGATGCTCACCGTCGAGGTTCTCAAAACACAAAATC
Mapping_targetC24G7
Source_location225CHROMOSOME_I40801304080130From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022886From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006820
TranscriptC09D1.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1b.1:c.20087+412T>A
Intron_number35/48
C09D1.1p.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1p.1:c.16508+412T>A
Intron_number25/37
C09D1.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1j.1:c.16748+412T>A
Intron_number24/36
C09D1.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1g.1:c.18668+412T>A
Intron_number26/38
C09D1.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1k.1:c.20021+412T>A
Intron_number34/46
C09D1.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1i.1:c.18602+412T>A
Intron_number25/37
C09D1.1n.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1n.1:c.17927+412T>A
Intron_number34/46
C09D1.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1h.1:c.16949+412T>A
Intron_number26/38
C09D1.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1f.1:c.18167+412T>A
Intron_number33/45
C09D1.1m.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1m.1:c.18368+412T>A
Intron_number35/47
MethodWGS_Flibotte