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WormBase Tree Display for Variation: WBVar01814063

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Name Class

WBVar01814063NamePublic_nameWBVar01814063
Other_namecewivar00525340
F56B6.2j.1:c.1705+96A>T
F56B6.2a.1:c.1696+96A>T
F56B6.2i.1:c.1702+96A>T
F56B6.2b.1:c.1585+96A>T
F56B6.2c.1:c.511+96A>T
F56B6.2h.1:c.1711+96A>T
F56B6.2e.1:c.211+96A>T
HGVSgCHROMOSOME_X:g.3550367A>T
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesAAAAAAAAATTTTGGAAAGTGTTTTTTTTTAATTTTCGAGTCAAAAATCGTTGAAAAATC
Mapping_targetF56B6
Source_location225CHROMOSOME_X35503543550354From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
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.1705+96A>T
Intron_number9/14
F56B6.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2e.1:c.211+96A>T
Intron_number1/7
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1702+96A>T
Intron_number10/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1585+96A>T
Intron_number9/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1696+96A>T
Intron_number10/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1711+96A>T
Intron_number10/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.511+96A>T
Intron_number4/9
MethodWGS_Flibotte