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WormBase Tree Display for Variation: WBVar01134633

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Name Class

WBVar01134633NamePublic_namegk493894
Other_nameF56B6.2h.1:c.1953-1661T>G
F56B6.2j.1:c.1947-1661T>G
F56B6.2c.1:c.753-1661T>G
F56B6.2e.1:c.453-1661T>G
F56B6.2i.1:c.1944-1661T>G
F56B6.2b.1:c.1827-1661T>G
F56B6.2a.1:c.1938-1661T>G
HGVSgCHROMOSOME_X:g.3554779T>G
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesCAAGCCAATTTTATAAAACACATACTTCTATCTAGCTCAAACAAATCTCGTATAATTGAATAATGTCGCAAAAAAATTGGGCAGATTTTTCCACTTTACG
Mapping_targetF56B6
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00039150
LaboratoryVC
AnalysisMillion_Mutation_Project
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.1947-1661T>G
Intron_number11/14
F56B6.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2e.1:c.453-1661T>G
Intron_number3/7
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1944-1661T>G
Intron_number12/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1827-1661T>G
Intron_number11/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1938-1661T>G
Intron_number12/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1953-1661T>G
Intron_number12/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.753-1661T>G
Intron_number6/9
ReferenceWBPaper00042537
MethodMillion_mutation