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WormBase Tree Display for Variation: WBVar01471099

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Name Class

WBVar01471099EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01471099
Other_namecewivar00613340
C34F6.10c.1:c.102-938C>A
C34F6.10a.1:c.-16-269C>A
C34F6.10d.1:c.-16-269C>A
C34F6.10b.1:c.102-938C>A
HGVSgCHROMOSOME_X:g.11237650G>T
Sequence_detailsSMapS_parentSequenceC03A3
Flanking_sequencesTTAAGCCTCGCATAAAATCGTAGCACATAGGTTCTAGGAATTGGCGTAGGCACTAAGAAA
Mapping_targetC03A3
Type_of_mutationSubstitutiongt
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00024204From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_rsrs193356401
dbSNP_ssss295532320
StatusLive
AffectsGeneWBGene00007944
TranscriptC34F6.10d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10d.1:c.-16-269C>A
Intron_number1/16
C34F6.10c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10c.1:c.102-938C>A
Intron_number2/15
C34F6.10b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10b.1:c.102-938C>A
Intron_number2/16
C34F6.10a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10a.1:c.-16-269C>A
Intron_number1/17
ReferenceWBPaper00040707
MethodWGS_Andersen