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WormBase Tree Display for Variation: WBVar01276498

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Name Class

WBVar01276498EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01276498
Other_namecewivar00255782
CE16419:p.Tyr9=
T19C9.2.1:c.27C>T
T19C9.5.1:c.-986G>A
HGVSgCHROMOSOME_V:g.17226193G>A
Sequence_detailsSMapS_parentSequenceT19C9
Flanking_sequencesCACGTGGCAAGAATGTTATAGGGTAGATTACATTTTGAGTAATTCGTTGCTAATACTGCTCTAACGCTGTGGGCATAGTTTAGACGTTAATGGAAAATTA
Mapping_targetT19C9
Type_of_mutationSubstitutiongAPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539110791
StatusLive
AffectsGeneWBGene00005331
WBGene00011841
TranscriptT19C9.5.1VEP_consequence5_prime_UTR_variant
VEP_impactMODIFIER
HGVScT19C9.5.1:c.-986G>A
cDNA_position505
Exon_number1/6
T19C9.2.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT19C9.2.1:c.27C>T
HGVSpCE16419:p.Tyr9=
cDNA_position27
CDS_position27
Protein_position9
Exon_number1/2
Codon_changetaC/taT
Amino_acid_changeY
ReferenceWBPaper00037807
MethodWGS_De_Bono