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WormBase Tree Display for Variation: WBVar01435642

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Name Class

WBVar01435642EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01435642
Other_namecewivar00303511
CE13367:p.Ile786=
T07D3.7b.1:c.2358C>T
CE32063:p.Ile805=
T07D3.7a.1:c.2415C>T
HGVSgCHROMOSOME_II:g.877707C>T
Sequence_detailsSMapS_parentSequenceT07D3
Flanking_sequencesCGACTTCTTCCTCTGCTCCCACGCTGGTATCAAGGAACATCCCGACCATCTCACTACCAT
Mapping_targetT07D3
Type_of_mutationSubstitutionct
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00005305From_analysisWGS_Andersen
WBStrain00005315From_analysisWGS_Andersen
WBStrain00005834From_analysisWGS_Andersen
WBStrain00006616From_analysisWGS_Andersen
WBStrain00006618From_analysisWGS_Andersen
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00023065From_analysisWGS_Andersen
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00027664From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193323704
dbSNP_ssss295499622
StatusLive
AffectsGeneWBGene00000106
TranscriptT07D3.7b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT07D3.7b.1:c.2358C>T
HGVSpCE13367:p.Ile786=
cDNA_position2360
CDS_position2358
Protein_position786
Exon_number6/8
Codon_changeatC/atT
Amino_acid_changeI
T07D3.7a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT07D3.7a.1:c.2415C>T
HGVSpCE32063:p.Ile805=
cDNA_position2415
CDS_position2415
Protein_position805
Exon_number6/8
Codon_changeatC/atT
Amino_acid_changeI
ReferenceWBPaper00040707
MethodWGS_Andersen