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WormBase Tree Display for Variation: WBVar01627805

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Name Class

WBVar01627805NamePublic_nameWBVar01627805
Other_namecewivar00309011
E02H9.3a.1:c.39+64A>T
E02H9.3a.2:c.39+64A>T
E02H9.3b.1:c.39+64A>T
HGVSgCHROMOSOME_III:g.2462109A>T
Sequence_detailsSMapS_parentSequenceE02H9
Flanking_sequencesTTCGATTTTCTCCTCATTTTTTTAAAAATTTTTTTTTTTTCGAAAAATCGATAAAAATTGATGATTATCGATTTTCATCCTAAACCCCCAGAAAAATCAATAATTTCTTTTTCAGAATTACGATTATCTGGTCCCACGTG
Mapping_targetE02H9
Source_location225CHROMOSOME_III24620992462099From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00017101
TranscriptE02H9.3a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScE02H9.3a.2:c.39+64A>T
Intron_number3/9
E02H9.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScE02H9.3a.1:c.39+64A>T
Intron_number2/8
E02H9.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScE02H9.3b.1:c.39+64A>T
Intron_number1/6
MethodWGS_Flibotte