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WormBase Tree Display for Variation: WBVar00553082

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Name Class

WBVar00553082NamePublic_nameWBVar00553082
Other_namehaw133217
cewivar00095285
C05D12.3c.3:c.2296T>G
CE36974:p.Ser766Ala
CE39469:p.Ser766Ala
C05D12.3c.1:c.2296T>G
C05D12.3a.1:c.2296T>G
C05D12.3c.2:c.2296T>G
HGVSgCHROMOSOME_II:g.11428999T>G
Sequence_detailsSMapS_parentSequenceC05D12
Flanking_sequencesTATTCCAATTTATTGGAACTGGAATCAAGGATATTTCCATCACTGACGCGCTGGAAAATCAGTTTCAGTAGATTCTAACACTCGATTCCAAAATGGGAAT
Mapping_targetC05D12
Type_of_mutationSubstitutiontg
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (36)
LaboratoryAX
PersonWBPerson4037
AnalysisWGS_Yanai
WGS_De_Bono
Million_mutation_project_reanalysis
HistoryAcquires_mergeWBVar01311924
WBVar01244857
WBVar01376773
StatusLive
AffectsGeneWBGene00014666
TranscriptC05D12.3a.1VEP_consequencemissense_variant
VEP_impactMODERATE
HGVScC05D12.3a.1:c.2296T>G
HGVSpCE36974:p.Ser766Ala
cDNA_position2308
CDS_position2296
Protein_position766
Exon_number11/16
Codon_changeTct/Gct
Amino_acid_changeS/A
C05D12.3c.1VEP_consequencemissense_variant
VEP_impactMODERATE
HGVScC05D12.3c.1:c.2296T>G
HGVSpCE39469:p.Ser766Ala
cDNA_position2311
CDS_position2296
Protein_position766
Exon_number11/18
Codon_changeTct/Gct
Amino_acid_changeS/A
C05D12.3c.3VEP_consequencemissense_variant
VEP_impactMODERATE
HGVScC05D12.3c.3:c.2296T>G
HGVSpCE39469:p.Ser766Ala
cDNA_position2296
CDS_position2296
Protein_position766
Exon_number10/18
Codon_changeTct/Gct
Amino_acid_changeS/A
C05D12.3c.2VEP_consequencemissense_variant
VEP_impactMODERATE
HGVScC05D12.3c.2:c.2296T>G
HGVSpCE39469:p.Ser766Ala
cDNA_position2310
CDS_position2296
Protein_position766
Exon_number11/17
Codon_changeTct/Gct
Amino_acid_changeS/A
ReferenceWBPaper00038208
WBPaper00037807
MethodWGS_Yanai