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WormBase Tree Display for Variation: WBVar01650010

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Name Class

WBVar01650010NamePublic_nameWBVar01650010
Other_namecewivar00336828
C11D2.6o.1:c.80-3621C>T
C11D2.6n.1:c.80-3621C>T
C11D2.6p.1:c.80-3621C>T
C11D2.6m.1:c.80-3621C>T
C11D2.6l.1:c.26-3621C>T
C11D2.6i.1:c.26-3621C>T
C11D2.6j.1:c.26-3621C>T
C11D2.6k.1:c.26-3621C>T
HGVSgCHROMOSOME_IV:g.6175027G>A
Sequence_detailsSMapS_parentSequenceC11D2
Flanking_sequencesATAAATGCTCAGTTTTATGTTCGGTTCAAAAGAAAAGTGAACTTTTTGTTTGGGACAAAA
Mapping_targetC11D2
Source_location225CHROMOSOME_IV61750166175016From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006809
TranscriptC11D2.6o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6o.1:c.80-3621C>T
Intron_number2/28
C11D2.6p.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6p.1:c.80-3621C>T
Intron_number2/28
C11D2.6i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6i.1:c.26-3621C>T
Intron_number1/28
C11D2.6l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6l.1:c.26-3621C>T
Intron_number1/27
C11D2.6n.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6n.1:c.80-3621C>T
Intron_number2/27
C11D2.6j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6j.1:c.26-3621C>T
Intron_number1/26
C11D2.6m.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6m.1:c.80-3621C>T
Intron_number2/29
C11D2.6k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6k.1:c.26-3621C>T
Intron_number1/27
MethodWGS_Flibotte