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WormBase Tree Display for Variation: WBVar01604549

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Name Class

WBVar01604549NamePublic_nameWBVar01604549
Other_namecewivar00281238
F52H3.1.4:c.2092+709T>C
F52H3.1.3:c.2092+709T>C
F52H3.1.1:c.2092+709T>C
F52H3.1.2:c.2092+709T>C
HGVSgCHROMOSOME_II:g.10034520A>G
Sequence_detailsSMapS_parentSequenceF52H3
Flanking_sequencesGAAACAATTTTCCATACTCAGGTTATCCAATTTCGCCATGATTTTTCTTACTTAATTTAA
Mapping_targetF52H3
Source_location225CHROMOSOME_II1003446110034461From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00002497
TranscriptF52H3.1.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF52H3.1.3:c.2092+709T>C
Intron_number10/11
F52H3.1.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF52H3.1.1:c.2092+709T>C
Intron_number10/11
F52H3.1.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF52H3.1.2:c.2092+709T>C
Intron_number10/11
F52H3.1.4VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF52H3.1.4:c.2092+709T>C
Intron_number9/10
MethodWGS_Flibotte