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: WBVar01825061

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01825061NamePublic_nameWBVar01825061
Other_namecewivar00536962
F56B6.2i.1:c.159-307C>T
F56B6.2a.1:c.159-307C>T
F56B6.2j.1:c.159-307C>T
F56B6.2h.1:c.159-307C>T
HGVSgCHROMOSOME_X:g.3545249C>T
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesTGTTTTCACTCCCTAATTAGCTCATCTTTTTGTACTTAGCGAACACGTGTCATTTGCAAT
Mapping_targetF56B6
Source_location225CHROMOSOME_X35452363545236From_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
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.159-307C>T
Intron_number2/14
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.159-307C>T
Intron_number3/16
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.159-307C>T
Intron_number3/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.159-307C>T
Intron_number3/16
MethodWGS_Flibotte