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WormBase Tree Display for Variation: WBVar02133167

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Name Class

WBVar02133167EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh16158
Other_nameF18F11.3e.1:c.256-1366T>A
F18F11.3c.1:c.256-1366T>A
F18F11.3b.1:c.256-1366T>A
F18F11.3f.1:c.256-1366T>A
F18F11.3g.1:c.256-1366T>A
F18F11.3a.1:c.256-1366T>A
F18F11.3d.1:c.256-1366T>A
F18F11.3h.1:c.256-1366T>A
HGVSgCHROMOSOME_IV:g.343807T>A
Sequence_detailsSMapS_parentSequenceF18F11
Flanking_sequencesCTGCTACGGAGTGTCATCAGTGGGTAGACACTTATTATAGAGAAAAAACAATACCTGAAACAAATACTCCAAAAAAAATT
Mapping_targetCHROMOSOME_IV
Source_location200CHROMOSOME_IV343807343807
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023750
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00017576
TranscriptF18F11.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3e.1:c.256-1366T>A
Intron_number3/25
F18F11.3g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3g.1:c.256-1366T>A
Intron_number3/25
F18F11.3f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3f.1:c.256-1366T>A
Intron_number3/24
F18F11.3h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3h.1:c.256-1366T>A
Intron_number3/26
F18F11.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3d.1:c.256-1366T>A
Intron_number3/25
F18F11.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3a.1:c.256-1366T>A
Intron_number3/25
F18F11.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3b.1:c.256-1366T>A
Intron_number3/23
F18F11.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3c.1:c.256-1366T>A
Intron_number3/24
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose