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WormBase Tree Display for Variation: WBVar01690361

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Name Class

WBVar01690361NamePublic_nameWBVar01690361
Other_namecewivar00382398
C34F6.10a.1:c.-16-1180A>C
C34F6.10b.1:c.102-1849A>C
C34F6.10d.1:c.-16-1180A>C
C34F6.10c.1:c.102-1849A>C
HGVSgCHROMOSOME_X:g.11238561T>G
Sequence_detailsSMapS_parentSequenceC03A3
Flanking_sequencesACGAAATCGAAAAGAACACTGGAGAATTTTTATTGGATTTAGATGAAATCGTCTATATTT
Mapping_targetC03A3
Source_location225CHROMOSOME_X1123849611238496From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00007944
TranscriptC34F6.10d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10d.1:c.-16-1180A>C
Intron_number1/16
C34F6.10c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10c.1:c.102-1849A>C
Intron_number2/15
C34F6.10b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10b.1:c.102-1849A>C
Intron_number2/16
C34F6.10a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC34F6.10a.1:c.-16-1180A>C
Intron_number1/17
MethodWGS_Flibotte