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WormBase Tree Display for Variation: WBVar01825219

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Name Class

WBVar01825219NamePublic_nameWBVar01825219
Other_namecewivar00537123
F39C12.3a.3:c.639+111G>A
F39C12.3b.1:c.711+111G>A
F39C12.3a.2:c.639+111G>A
F39C12.3a.1:c.639+111G>A
HGVSgCHROMOSOME_X:g.4868755C>T
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesATTTTTTATTGGTTCATCGCCTAGTATTACCGTGTTATTTTGGAACTTTGTAGAAGTGCC
Mapping_targetF39C12
Source_location225CHROMOSOME_X48687254868725From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006640
TranscriptF39C12.3a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.3:c.639+111G>A
Intron_number7/10
F39C12.3a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.2:c.639+111G>A
Intron_number6/9
F39C12.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.1:c.639+111G>A
Intron_number7/10
F39C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3b.1:c.711+111G>A
Intron_number7/9
MethodWGS_Flibotte