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WormBase Tree Display for Variation: WBVar01389877

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Name Class

WBVar01389877EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01389877
Other_namecewivar00192429
T12B5.6b.1:c.30G>A
CE51680:p.Gln10=
T12B5.6c.1:c.30G>A
CE39403:p.Gln10=
HGVSgCHROMOSOME_III:g.936038C>T
Sequence_detailsSMapS_parentSequenceT12B5
Flanking_sequencesTTAGCGATATTTAAAGGCATATTGAGAAAAGTTGGCAATACCAGATTTTTTGATGTGTCTTCGGCGCGATATCGGTCATTTTAGAAAGTTCCTGAAAAAC
Mapping_targetT12B5
Type_of_mutationSubstitutioncTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
WBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539065328
StatusLive
AffectsGeneWBGene00020453
TranscriptT12B5.6c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT12B5.6c.1:c.30G>A
HGVSpCE51680:p.Gln10=
cDNA_position48
CDS_position30
Protein_position10
Exon_number2/5
Codon_changecaG/caA
Amino_acid_changeQ
T12B5.6b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScT12B5.6b.1:c.30G>A
HGVSpCE39403:p.Gln10=
cDNA_position50
CDS_position30
Protein_position10
Exon_number2/5
Codon_changecaG/caA
Amino_acid_changeQ
ReferenceWBPaper00037807
MethodWGS_De_Bono