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WormBase Tree Display for Variation: WBVar01835008

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Name Class

WBVar01835008NamePublic_nameWBVar01835008
Other_namecewivar00547326
C34E11.2e.1:c.1881+85C>G
C34E11.2d.1:c.1556+214C>G
C34E11.2g.1:c.1514-217C>G
C34E11.2f.1:c.1599+85C>G
C34E11.2b.1:c.1571+214C>G
C34E11.2a.1:c.1838+214C>G
C34E11.2c.1:c.1739+214C>G
HGVSgCHROMOSOME_X:g.11807660G>C
Sequence_detailsSMapS_parentSequenceC34E11
Flanking_sequencesAACAGAGGGAATGAGGCGTTGGCGTGGGTAAATACAAAAGTGAATTGAAAAGCAACAAAA
Mapping_targetC34E11
Source_location225CHROMOSOME_X1180759211807592From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022899From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00007935
TranscriptC34E11.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2c.1:c.1739+214C>G
Intron_number11/13
C34E11.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2g.1:c.1514-217C>G
Intron_number10/12
C34E11.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2b.1:c.1571+214C>G
Intron_number10/12
C34E11.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2a.1:c.1838+214C>G
Intron_number12/15
C34E11.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2f.1:c.1599+85C>G
Intron_number13/15
C34E11.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2e.1:c.1881+85C>G
Intron_number13/15
C34E11.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34E11.2d.1:c.1556+214C>G
Intron_number11/14
MethodWGS_Flibotte