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WormBase Tree Display for Variation: WBVar01817029

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Name Class

WBVar01817029NamePublic_nameWBVar01817029
Other_namecewivar00528474
F16H9.2a.1:c.-23-16020A>C
F16H9.2b.1:c.35-16020A>C
F16H9.1a.1:c.47+1194T>G
F16H9.1c.1:c.26+903T>G
F16H9.1b.1:c.84-2316T>G
HGVSgCHROMOSOME_X:g.12723323T>G
Sequence_detailsSMapS_parentSequenceF16H9
Flanking_sequencesTGTGAAGCTTCGTACGGAGTTCAGTGTGCTGAATTTCTTCCATAAGTTCATGAATCTTTG
Mapping_targetF16H9
Source_location225CHROMOSOME_X1272325212723252From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00008901
WBGene00004345
TranscriptF16H9.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.1a.1:c.47+1194T>G
Intron_number2/6
F16H9.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.2b.1:c.35-16020A>C
Intron_number1/3
F16H9.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.1c.1:c.26+903T>G
Intron_number2/6
F16H9.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.2a.1:c.-23-16020A>C
Intron_number1/4
F16H9.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.1b.1:c.84-2316T>G
Intron_number2/6
MethodWGS_Flibotte