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WormBase Tree Display for Variation: WBVar01646692

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Name Class

WBVar01646692NamePublic_nameWBVar01646692
Other_namecewivar00333330
Y41C4A.4f.1:c.257-332T>C
Y41C4A.4g.1:c.974-332T>C
Y41C4A.4d.1:c.683-332T>C
Y41C4A.4e.1:c.608-332T>C
Y41C4A.4b.1:c.671-332T>C
Y41C4A.4a.1:c.665-332T>C
Y41C4A.4c.1:c.632-332T>C
HGVSgCHROMOSOME_III:g.11692149T>C
Sequence_detailsSMapS_parentSequenceY41C4A
Flanking_sequencesATTTTTGTGGTAAAAAATTTATTTTAAAAATGTTCTTTATAGAGTATAATATACAAGCTA
Mapping_targetY41C4A
Source_location225CHROMOSOME_III1169204911692049From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000793
TranscriptY41C4A.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4e.1:c.608-332T>C
Intron_number6/8
Y41C4A.4g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4g.1:c.974-332T>C
Intron_number4/6
Y41C4A.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4b.1:c.671-332T>C
Intron_number5/6
Y41C4A.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4a.1:c.665-332T>C
Intron_number6/8
Y41C4A.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4d.1:c.683-332T>C
Intron_number6/8
Y41C4A.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4f.1:c.257-332T>C
Intron_number3/5
Y41C4A.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4c.1:c.632-332T>C
Intron_number5/6
MethodWGS_Flibotte