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WormBase Tree Display for Variation: WBVar02130684

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Name Class

WBVar02130684EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh6951
Other_nameC09D8.1j.1:c.865+980G>A
C09D8.1f.1:c.733+980G>A
C09D8.1i.1:c.865+980G>A
C09D8.1k.1:c.733+980G>A
C09D8.1a.1:c.733+980G>A
C09D8.1l.1:c.733+980G>A
HGVSgCHROMOSOME_II:g.10978210G>A
Sequence_detailsSMapS_parentSequenceC09D8
Flanking_sequencesGAAATAGTTTGAGCTTCTAAGCATTTTTAGTCAAAATTTTGAAAAGTGCCAACCTTTCAAAACAAAAGTGTAAATTTTGG
Mapping_targetCHROMOSOME_II
Source_location200CHROMOSOME_II1097813410978134
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023732
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00004215
TranscriptC09D8.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D8.1i.1:c.865+980G>A
Intron_number4/27
C09D8.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D8.1j.1:c.865+980G>A
Intron_number4/28
C09D8.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D8.1a.1:c.733+980G>A
Intron_number4/28
C09D8.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D8.1k.1:c.733+980G>A
Intron_number4/27
C09D8.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D8.1f.1:c.733+980G>A
Intron_number4/28
C09D8.1l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09D8.1l.1:c.733+980G>A
Intron_number4/29
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose