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WormBase Tree Display for Variation: WBVar01552094

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Name Class

WBVar01552094NamePublic_nameWBVar01552094
Other_namecewivar00129201
CE43855:p.Asn105Asp
F31B12.1k.1:c.4269+479A>G
F31B12.1i.1:c.4239+479A>G
F31B12.1l.1:c.4098+479A>G
F31B12.1j.1:c.4068+479A>G
F31B12.1g.1:c.4089+479A>G
F31B12.3.1:c.313A>G
F31B12.1h.1:c.4119+479A>G
F31B12.1d.1:c.4260+479A>G
HGVSgCHROMOSOME_X:g.10820254T>C
Sequence_detailsSMapS_parentSequenceF31B12
Flanking_sequencesAAAAGGGCTTACCAATTGAAGAATGTTCATATAGTTGGAAATAAACTCTTCTAGGTTTCG
Mapping_targetF31B12
Source_location225CHROMOSOME_X1082018910820189From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (11)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001495
WBGene00004036
TranscriptF31B12.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1j.1:c.4068+479A>G
Intron_number27/63
F31B12.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1h.1:c.4119+479A>G
Intron_number27/63
F31B12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1d.1:c.4260+479A>G
Intron_number28/64
F31B12.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1g.1:c.4089+479A>G
Intron_number27/63
F31B12.1l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1l.1:c.4098+479A>G
Intron_number27/63
F31B12.3.1 (12)
F31B12.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1i.1:c.4239+479A>G
Intron_number28/64
F31B12.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF31B12.1k.1:c.4269+479A>G
Intron_number28/64
MethodWGS_Flibotte