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WormBase Tree Display for Variation: WBVar01551930

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Name Class

WBVar01551930NamePublic_nameWBVar01551930
Other_namecewivar00129014
F14F3.1c.1:c.310-71T>C
F14F3.1b.1:c.229-71T>C
F14F3.1a.1:c.787-71T>C
F14F3.1a.2:c.787-71T>C
HGVSgCHROMOSOME_X:g.10517353T>C
Sequence_detailsSMapS_parentSequenceF14F3
Flanking_sequencesTGCCAGCTGAGAAAGGTTGGGTCGGGTGGTTATATCAAACAATTCAAATTTCGAAATCAA
Mapping_targetF14F3
Source_location225CHROMOSOME_X1051729110517291From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006870
TranscriptF14F3.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF14F3.1c.1:c.310-71T>C
Intron_number4/7
F14F3.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF14F3.1a.1:c.787-71T>C
Intron_number10/13
F14F3.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF14F3.1a.2:c.787-71T>C
Intron_number9/12
F14F3.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF14F3.1b.1:c.229-71T>C
Intron_number3/5
MethodWGS_Flibotte