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WormBase Tree Display for Variation: WBVar02097949

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Name Class

WBVar02097949NamePublic_nameWBVar02097949
Other_namecewivar00828072
F57H12.4.2:c.-130-189_-130-164delinsAAAAAATTTGTATTTTTAACAAGTAC
F57H12.4.1:c.-607-190_-607-165delinsAAAAAATTTGTATTTTTAACAAGTAC
F57H12.4.3:c.-129-190_-129-165delinsAAAAAATTTGTATTTTTAACAAGTAC
HGVSgCHROMOSOME_IV:g.7970342_7970367delinsAAAAAATTTGTATTTTTAACAAGTAC
Sequence_detailsSMapS_parentSequenceF57H12
Flanking_sequencesCGAAGACCGAGTTCCATTTTTGGCAAATTATCATTCAAAAAATTTGCCCCCTTTGAGACT
Mapping_targetF57H12
Source_location225CHROMOSOME_IV79703307970355From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionAAAAAATTTGTATTTTTAACAAGTAC
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019019
TranscriptF57H12.4.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF57H12.4.1:c.-607-190_-607-165delinsAAAAAATTTGTATTTTTAACAAGTAC
Intron_number1/8
F57H12.4.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF57H12.4.3:c.-129-190_-129-165delinsAAAAAATTTGTATTTTTAACAAGTAC
Intron_number1/9
F57H12.4.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF57H12.4.2:c.-130-189_-130-164delinsAAAAAATTTGTATTTTTAACAAGTAC
Intron_number1/9
MethodWGS_Flibotte