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WormBase Tree Display for Variation: WBVar00602751

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Name Class

WBVar00602751NamePublic_nameWBVar00602751
Other_nameoicr_ce1170
cewivar00018433
T12B5.6c.1:c.114-14T>C
T12B5.6b.1:c.187T>C
CE39403:p.Tyr63His
HGVSgCHROMOSOME_III:g.934393A>G
Sequence_detailsSMapS_parentSequenceT12B5
Flanking_sequencesTGTCATTTTCTGCTGTATTATATATGATTTCAGTTCCACTCCATATTTCGACTTCATCTTTCCTCAAGTACAAATGATGTAGTCAAAACGTAATCCAATTTTATCGACAGCAGTTCTCAAACTGCGACAGACTTTTCTCGCTCTCAGTCT
Mapping_targetT12B5
Type_of_mutationSubstitutionag
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000032From_analysisMillion_mutation_project_reanalysis
WGS_Stein
WBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
AnalysisWGS_Stein
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssssss477719671
StatusLive
AffectsGeneWBGene00020453
TranscriptT12B5.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT12B5.6c.1:c.114-14T>C
Intron_number2/4
T12B5.6b.1 (12)
Remarkvalidatation rate is over 97%
MethodWGS_Stein