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WormBase Tree Display for Variation: WBVar01702795

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Name Class

WBVar01702795NamePublic_nameWBVar01702795
Other_namecewivar00400139
Y41D4A.4c.1:c.728+387A>T
Y41D4A.4b.1:c.941+387A>T
Y41D4A.4e.1:c.932+387A>T
Y41D4A.4a.1:c.932+387A>T
HGVSgCHROMOSOME_IV:g.1748704A>T
Sequence_detailsSMapS_parentSequenceY41D4A
Flanking_sequencesTTTAAATTTCTATGAAAAAGCTGATTTTTGAAATGCTGAAATTTTAAATTTCTATGAAAA
Mapping_targetY41D4A
Source_location225CHROMOSOME_IV17487031748703From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021506
TranscriptY41D4A.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41D4A.4e.1:c.932+387A>T
Intron_number4/5
Y41D4A.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41D4A.4b.1:c.941+387A>T
Intron_number4/5
Y41D4A.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41D4A.4a.1:c.932+387A>T
Intron_number5/7
Y41D4A.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41D4A.4c.1:c.728+387A>T
Intron_number3/4
MethodWGS_Flibotte