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WormBase Tree Display for Variation: WBVar01711048

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Name Class

WBVar01711048NamePublic_nameWBVar01711048
Other_namecewivar00408723
F39C12.2e.1:c.756+110A>G
F39C12.2c.1:c.756+110A>G
F39C12.2a.1:c.756+110A>G
F39C12.2d.1:c.756+110A>G
F39C12.2b.1:c.756+110A>G
HGVSgCHROMOSOME_X:g.4858097T>C
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesAAAAAACGGTTGCCGATTTTGCTTCTAGTTCTTTAACCTTCAGATTTTCAATTTTCTCTC
Mapping_targetF39C12
Source_location225CHROMOSOME_X48580674858067From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (11)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000072
TranscriptF39C12.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2b.1:c.756+110A>G
Intron_number7/19
F39C12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2a.1:c.756+110A>G
Intron_number6/16
F39C12.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2c.1:c.756+110A>G
Intron_number7/18
F39C12.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2e.1:c.756+110A>G
Intron_number6/15
F39C12.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2d.1:c.756+110A>G
Intron_number6/16
MethodWGS_Flibotte