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WormBase Tree Display for Variation: WBVar01620963

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Name Class

WBVar01620963NamePublic_nameWBVar01620963
Other_namecewivar00300684
C34E11.2a.1:c.1796-287A>T
C34E11.2f.1:c.1514-287A>T
C34E11.2b.1:c.1529-287A>T
C34E11.2g.1:c.1514-760A>T
C34E11.2e.1:c.1796-287A>T
C34E11.2c.1:c.1697-287A>T
C34E11.2d.1:c.1514-287A>T
HGVSgCHROMOSOME_X:g.11808203T>A
Sequence_detailsSMapS_parentSequenceC34E11
Flanking_sequencesTTTTCAGAGGAACATTGCAAAATAAGCATATCCAATGTTAACTTCAAGCAATATTTGTTA
Mapping_targetC34E11
Source_location225CHROMOSOME_X1180813511808135From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (15)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00007935
TranscriptC34E11.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2c.1:c.1697-287A>T
Intron_number10/13
C34E11.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2g.1:c.1514-760A>T
Intron_number10/12
C34E11.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2b.1:c.1529-287A>T
Intron_number9/12
C34E11.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2a.1:c.1796-287A>T
Intron_number11/15
C34E11.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2f.1:c.1514-287A>T
Intron_number11/15
C34E11.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2e.1:c.1796-287A>T
Intron_number11/15
C34E11.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2d.1:c.1514-287A>T
Intron_number10/14
MethodWGS_Flibotte