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WormBase Tree Display for Variation: WBVar02004941

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Name Class

WBVar02004941NamePublic_nameWBVar02004941
Other_namecewivar00732533
T28F12.2c.1:c.-1807+489del
T28F12.2a.1:c.123+489del
T28F12.2d.2:c.-1243+489del
T28F12.2d.1:c.-1225+489del
T28F12.2f.1:c.123+489del
HGVSgCHROMOSOME_V:g.4498078del
Sequence_detailsSMapS_parentSequenceT28F12
Flanking_sequencesGGTCTCGCCACAGGAGCTAAATTCAACAGATTTTTTTCATTTGACATAGGAAAACAAATT
Mapping_targetT28F12
Source_location225CHROMOSOME_V44980644498064From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006796
TranscriptT28F12.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2c.1:c.-1807+489del
Intron_number1/10
T28F12.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2d.1:c.-1225+489del
Intron_number1/11
T28F12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2a.1:c.123+489del
Intron_number2/11
T28F12.2d.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2d.2:c.-1243+489del
Intron_number1/11
T28F12.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT28F12.2f.1:c.123+489del
Intron_number2/10
MethodWGS_Flibotte