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WormBase Tree Display for Variation: WBVar00270773

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Name Class

WBVar00270773EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00270773
Other_nameuCE4-1153
CE44609:p.Ala73LeufsTer4
K01A6.2e.1:c.217del
K01A6.2d.1:c.180-131del
K01A6.2c.1:c.936-131del
K01A6.2a.1:c.936-131del
K01A6.2b.1:c.339-131del
HGVSgCHROMOSOME_IV:g.11724825del
Sequence_detailsSMapS_parentSequenceK01A6
Flanking_sequencesAACACAGACAACGTTTGATGGTGGAAGTAATAGGCACAAGGGTTTTGTTTCGTTTCGATCACAAGATGAAGATCAGAATGAAGATGATTGTGAAGAAGGGCTCTTTTGTTGAAAGCTGTTCAGCATACATCATCGGCAAAAAAGTATGACCACTGATACAAAACCTAGACAACTAATTTAGAAATTTTCATTAAGGACAA
Mapping_targetK01A6
Type_of_mutationDeletionG
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
AnalysisSNP_Swan
StatusLive
AffectsGeneWBGene00010444
TranscriptK01A6.2e.1VEP_consequenceframeshift_variant
VEP_impactHIGH
HGVScK01A6.2e.1:c.217del
HGVSpCE44609:p.Ala73LeufsTer4
cDNA_position217
CDS_position217
Protein_position73
Exon_number1/8
Codon_changeGct/ct
Amino_acid_changeA/X
K01A6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A6.2a.1:c.936-131del
Intron_number9/15
K01A6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A6.2c.1:c.936-131del
Intron_number9/16
K01A6.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A6.2d.1:c.180-131del
Intron_number3/9
K01A6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A6.2b.1:c.339-131del
Intron_number4/10
ReferenceWBPaper00005369
MethodSNP_Swan