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WormBase Tree Display for Variation: WBVar01690362

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Name Class

WBVar01690362NamePublic_nameWBVar01690362
Other_namecewivar00382399
C34F6.10c.1:c.101+963G>A
C34F6.10a.1:c.-17+963G>A
C34F6.10d.1:c.-17+963G>A
C34F6.10b.1:c.101+963G>A
HGVSgCHROMOSOME_X:g.11239547C>T
Sequence_detailsSMapS_parentSequenceC03A3
Flanking_sequencesATCTGCCCACACAAGTAGGCATCATTTGTGCCTTTCCTCATGGGGCGACGAGAAAAAAAA
Mapping_targetC03A3
Source_location225CHROMOSOME_X1123948211239482From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00007944
TranscriptC34F6.10d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10d.1:c.-17+963G>A
Intron_number1/16
C34F6.10c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10c.1:c.101+963G>A
Intron_number2/15
C34F6.10b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10b.1:c.101+963G>A
Intron_number2/16
C34F6.10a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10a.1:c.-17+963G>A
Intron_number1/17
MethodWGS_Flibotte