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WormBase Tree Display for Variation: WBVar01655237

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Name Class

WBVar01655237NamePublic_nameWBVar01655237
Other_namecewivar00342369
F56D12.1c.1:c.679-287G>A
F56D12.1b.1:c.679-287G>A
F56D12.1d.1:c.259-287G>A
F56D12.1a.1:c.679-287G>A
F56D12.1a.2:c.679-287G>A
HGVSgCHROMOSOME_II:g.1308302C>T
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesAGCAGACCAAATTTCTTCAAAACTACTTGGGTCTGCTAAATCGAAACTTGTAGTTTGTAGCTAGCAGACCCAATTTCTTCAAAACTACTT
Mapping_targetF56D12
Source_location225CHROMOSOME_II13083091308309From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006631From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000112
TranscriptF56D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1b.1:c.679-287G>A
Intron_number5/7
F56D12.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.2:c.679-287G>A
Intron_number6/9
F56D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.1:c.679-287G>A
Intron_number5/8
F56D12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1d.1:c.259-287G>A
Intron_number1/3
F56D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1c.1:c.679-287G>A
Intron_number4/5
MethodWGS_Flibotte