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WormBase Tree Display for Variation: WBVar01533957

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Name Class

WBVar01533957NamePublic_nameWBVar01533957
Other_namecewivar00080062
F56D12.1c.1:c.1137+21C>G
F56D12.1b.1:c.1137+21C>G
F56D12.1d.1:c.717+21C>G
F56D12.1a.2:c.1137+21C>G
F56D12.1a.1:c.1137+21C>G
HGVSgCHROMOSOME_II:g.1307536G>C
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesACCTGTAAACTACAAACTACACAAAAATCGCAAGCCAAACAGTGGCCTACATCTCCAAGC
Mapping_targetF56D12
Source_location225CHROMOSOME_II13075431307543From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000112
TranscriptF56D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1b.1:c.1137+21C>G
Intron_number6/7
F56D12.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.2:c.1137+21C>G
Intron_number7/9
F56D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.1:c.1137+21C>G
Intron_number6/8
F56D12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1d.1:c.717+21C>G
Intron_number2/3
F56D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1c.1:c.1137+21C>G
Intron_number5/5
MethodWGS_Flibotte