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WormBase Tree Display for Variation: WBVar01814062

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Name Class

WBVar01814062NamePublic_nameWBVar01814062
Other_namecewivar00525339
F56B6.2j.1:c.426+57C>T
F56B6.2h.1:c.426+57C>T
F56B6.2i.1:c.426+57C>T
F56B6.2b.1:c.315+57C>T
F56B6.2a.1:c.426+57C>T
HGVSgCHROMOSOME_X:g.3545880C>T
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesTATCAGCGAAGTATTTCAAAGGTGTAGTAGGCATTCTATAGTATTAAAAAATGACCAAAT
Mapping_targetF56B6
Source_location225CHROMOSOME_X35458673545867From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.426+57C>T
Intron_number3/14
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.426+57C>T
Intron_number4/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.315+57C>T
Intron_number3/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.426+57C>T
Intron_number4/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.426+57C>T
Intron_number4/16
MethodWGS_Flibotte