Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01819582

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01819582NamePublic_nameWBVar01819582
Other_namecewivar00531185
F39C12.3b.1:c.35+697T>C
F39C12.3a.1:c.-38+697T>C
F39C12.3a.3:c.-37-2617T>C
HGVSgCHROMOSOME_X:g.4873676A>G
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesAATTTTCTTAGTTTAGAAAGATACCTTTCTAAATATTTCAACTTTGATTTATATGTAGAG
Mapping_targetF39C12
Source_location225CHROMOSOME_X48736464873646From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_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.-37-2617T>C
Intron_number1/10
F39C12.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.1:c.-38+697T>C
Intron_number1/10
F39C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3b.1:c.35+697T>C
Intron_number2/9
MethodWGS_Flibotte