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WormBase Tree Display for Variation: WBVar00266983

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Name Class

WBVar00266983EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00266983
Other_name (11)
HGVSgCHROMOSOME_I:g.4080035dup
Sequence_detailsSMapS_parentSequenceC24G7
Flanking_sequencesAAAATTACGAGTGCCAAATGCTGGCACTTAATAACTAAACATTGCGTAAAGTAAACAATTTTTAATTTGAATATAAAAGATCATCTCGCTAATTTTTTTTCTTCGAGAAGTTACAGGAAAATTGAAAGATGTCTACAATATTTATTCTGAATCCAAAGTAAGCCAATAATTTTTTTTTAATTCTGGCGATGCTTCACCGTC
Mapping_targetC24G7
Type_of_mutationInsertionT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
AnalysisSNP_Swan
StatusLive
AffectsGeneWBGene00006820
TranscriptC09D1.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1b.1:c.20087+319dup
Intron_number35/48
C09D1.1p.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1p.1:c.16508+319dup
Intron_number25/37
C09D1.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1j.1:c.16748+319dup
Intron_number24/36
C09D1.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1g.1:c.18668+319dup
Intron_number26/38
C09D1.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1k.1:c.20021+319dup
Intron_number34/46
C09D1.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1i.1:c.18602+319dup
Intron_number25/37
C09D1.1n.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1n.1:c.17927+319dup
Intron_number34/46
C09D1.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1h.1:c.16949+319dup
Intron_number26/38
C09D1.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1f.1:c.18167+319dup
Intron_number33/45
C09D1.1m.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D1.1m.1:c.18368+319dup
Intron_number35/47
ReferenceWBPaper00005369
MethodSNP_Swan