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WormBase Tree Display for Variation: WBVar01822319

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Name Class

WBVar01822319NamePublic_nameWBVar01822319
Other_namecewivar00534080
Y41G9A.4d.1:c.2147-161T>C
Y41G9A.4e.1:c.206-161T>C
Y41G9A.4c.1:c.2114-161T>C
Y41G9A.4b.1:c.2246-161T>C
HGVSgCHROMOSOME_X:g.2966947T>C
Sequence_detailsSMapS_parentSequenceY41G9A
Flanking_sequencesAGGATTATTGATTTTTTGTGTTTCAAAATGAGAAACAGTAATTTTATTACCTCACATAAT
Mapping_targetY41G9A
Source_location225CHROMOSOME_X29669372966937From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021528
TranscriptY41G9A.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4c.1:c.2114-161T>C
Intron_number16/20
Y41G9A.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4d.1:c.2147-161T>C
Intron_number16/19
Y41G9A.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4b.1:c.2246-161T>C
Intron_number17/21
Y41G9A.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41G9A.4e.1:c.206-161T>C
Intron_number1/4
MethodWGS_Flibotte