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WormBase Tree Display for Variation: WBVar01648513

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Name Class

WBVar01648513NamePublic_nameWBVar01648513
Other_namecewivar00335249
Y41D4A.4c.1:c.728+566C>T
Y41D4A.4e.1:c.932+566C>T
Y41D4A.4b.1:c.941+566C>T
Y41D4A.4a.1:c.932+566C>T
HGVSgCHROMOSOME_IV:g.1748883C>T
Sequence_detailsSMapS_parentSequenceY41D4A
Flanking_sequencesTTTTTTTTTTGAAAAATCACTGACTTTCCAAACAAAAGTGCTAAACCAATGTTTTAAAAG
Mapping_targetY41D4A
Source_location225CHROMOSOME_IV17488821748882From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021506
TranscriptY41D4A.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41D4A.4e.1:c.932+566C>T
Intron_number4/5
Y41D4A.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41D4A.4b.1:c.941+566C>T
Intron_number4/5
Y41D4A.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41D4A.4a.1:c.932+566C>T
Intron_number5/7
Y41D4A.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41D4A.4c.1:c.728+566C>T
Intron_number3/4
MethodWGS_Flibotte