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WormBase Tree Display for Variation: WBVar01549468

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Name Class

WBVar01549468NamePublic_nameWBVar01549468
Other_namecewivar00125630
F39C12.2b.1:c.99+24C>T
F39C12.2a.1:c.99+24C>T
F39C12.2c.1:c.99+24C>T
F39C12.2e.1:c.99+24C>T
F39C12.2d.1:c.99+24C>T
HGVSgCHROMOSOME_X:g.4859914G>A
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesGAAAACTTGATGTGCTCTAGTTTTTTTTACGAAAAACTTGGAGCAGCACTTACTTTGATT
Mapping_targetF39C12
Source_location225CHROMOSOME_X48598844859884From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000072
TranscriptF39C12.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2b.1:c.99+24C>T
Intron_number2/19
F39C12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2a.1:c.99+24C>T
Intron_number1/16
F39C12.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2c.1:c.99+24C>T
Intron_number2/18
F39C12.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2e.1:c.99+24C>T
Intron_number1/15
F39C12.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2d.1:c.99+24C>T
Intron_number1/16
MethodWGS_Flibotte