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WormBase Tree Display for Variation: WBVar00267183

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Name Class

WBVar00267183EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00267183
Other_nameuCE1-1027
F16A11.3d.1:c.927+3054_927+3055insA
F16A11.3b.1:c.711+3054_711+3055insA
F16A11.3a.1:c.711+3054_711+3055insA
F16A11.3c.1:c.711+3054_711+3055insA
HGVSgCHROMOSOME_I:g.9379417dup
Sequence_detailsSMapS_parentSequenceF16A11
Flanking_sequencesGACAGCTTTTTTCCGAGTGTTTTTTTTTTCATTCTCTCAGAAAAAAGGAGACCGGGGAAGGCATATGGTGGCAATCTGATGAAGAAAAACGTTTTTTTTTCTTCCGTCTTTTTTGTTCGTTTAGAGAAAACGGCAGATGGAAAGAAAGAAAAGAAGAAGGGTGTTCGTGTTCACAGTCTTCTTCCTCTTCCCGGCAACGAA
Mapping_targetF16A11
Type_of_mutationInsertionT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
AnalysisSNP_Swan
StatusLive
AffectsGeneWBGene00305537
WBGene00008878
TranscriptF16A11.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16A11.3c.1:c.711+3054_711+3055insA
Intron_number5/15
F16A11.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16A11.3a.1:c.711+3054_711+3055insA
Intron_number6/25
F16A11.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16A11.3b.1:c.711+3054_711+3055insA
Intron_number6/24
M04C9.10
F16A11.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16A11.3d.1:c.927+3054_927+3055insA
Intron_number7/25
ReferenceWBPaper00005369
MethodSNP_Swan