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WormBase Tree Display for Variation: WBVar02095969

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Name Class

WBVar02095969NamePublic_nameWBVar02095969
Other_namecewivar00826015
Y41C4A.4f.1:c.-49_-24delinsTATCGATAGGATCACATATTATTTTAA
Y41C4A.4e.1:c.391+1393_391+1418delinsTATCGATAGGATCACATATTATTTTAA
Y41C4A.4g.1:c.766+1393_766+1418delinsTATCGATAGGATCACATATTATTTTAA
Y41C4A.4d.1:c.466+1393_466+1418delinsTATCGATAGGATCACATATTATTTTAA
Y41C4A.4c.1:c.415+1393_415+1418delinsTATCGATAGGATCACATATTATTTTAA
Y41C4A.4b.1:c.454+1393_454+1418delinsTATCGATAGGATCACATATTATTTTAA
Y41C4A.4a.1:c.448+1393_448+1418delinsTATCGATAGGATCACATATTATTTTAA
HGVSgCHROMOSOME_III:g.11689729_11689754delinsTATCGATAGGATCACATATTATTTTAA
Sequence_detailsSMapS_parentSequenceY41C4A
Flanking_sequencesATCATCAGTTGACCGTATTATTATTATTATTTTTTTTTTGGTCTACAGTTTCAATGGAGT
Mapping_targetY41C4A
Source_location225CHROMOSOME_III1168962911689654From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionTATCGATAGGATCACATATTATTTTAA
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000793
TranscriptY41C4A.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4e.1:c.391+1393_391+1418delinsTATCGATAGGATCACATATTATTTTAA
Intron_number5/8
Y41C4A.4g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4g.1:c.766+1393_766+1418delinsTATCGATAGGATCACATATTATTTTAA
Intron_number3/6
Y41C4A.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4b.1:c.454+1393_454+1418delinsTATCGATAGGATCACATATTATTTTAA
Intron_number4/6
Y41C4A.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4a.1:c.448+1393_448+1418delinsTATCGATAGGATCACATATTATTTTAA
Intron_number5/8
Y41C4A.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4d.1:c.466+1393_466+1418delinsTATCGATAGGATCACATATTATTTTAA
Intron_number5/8
Y41C4A.4f.1VEP_consequence5_prime_UTR_variant
VEP_impactMODIFIER
HGVScY41C4A.4f.1:c.-49_-24delinsTATCGATAGGATCACATATTATTTTAA
cDNA_position218-243
Exon_number1/6
Y41C4A.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY41C4A.4c.1:c.415+1393_415+1418delinsTATCGATAGGATCACATATTATTTTAA
Intron_number4/6
MethodWGS_Flibotte