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WormBase Tree Display for Variation: WBVar01851260

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Name Class

WBVar01851260NamePublic_nameWBVar01851260
Other_namecewivar00564297
F45E10.1c.1:c.281-2388C>T
F45E10.1g.1:c.281-2388C>T
F45E10.1a.1:c.281-2388C>T
F45E10.1d.1:c.-122-2388C>T
F45E10.1b.1:c.281-2388C>T
F45E10.1h.1:c.281-2388C>T
HGVSgCHROMOSOME_II:g.11076269G>A
Sequence_detailsSMapS_parentSequenceC09H10
Flanking_sequencesTGAAATGATGCAGTGCACGCGCGGGAGACTTTTCGCTTTTTGACTAACGAGTGAGATGTC
Mapping_targetC09H10
Source_location225CHROMOSOME_II1107621111076211From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006788
TranscriptF45E10.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45E10.1c.1:c.281-2388C>T
Intron_number4/23
F45E10.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45E10.1b.1:c.281-2388C>T
Intron_number4/22
F45E10.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45E10.1d.1:c.-122-2388C>T
Intron_number1/20
F45E10.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45E10.1g.1:c.281-2388C>T
Intron_number4/21
F45E10.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45E10.1a.1:c.281-2388C>T
Intron_number5/23
F45E10.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45E10.1h.1:c.281-2388C>T
Intron_number4/21
MethodWGS_Flibotte