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WormBase Tree Display for Variation: WBVar01830916

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Name Class

WBVar01830916NamePublic_nameWBVar01830916
Other_namecewivar00543071
R07D5.1a.1:c.-8-5625C>T
R07D5.1g.1:c.18+1371C>T
R07D5.1c.1:c.-165-6032C>T
R07D5.1f.1:c.18+1371C>T
R07D5.1e.1:c.268-6032C>T
R07D5.1d.1:c.268-6032C>T
HGVSgCHROMOSOME_X:g.15133207G>A
Sequence_detailsSMapS_parentSequenceR07D5
Flanking_sequencesCTTGGAGTAAACGTCATTTTTGACCAAGAATCAGCTAGAACAACAAACATACAAAAAGCA
Mapping_targetR07D5
Source_location225CHROMOSOME_X1513313715133137From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022886From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006747
TranscriptR07D5.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1f.1:c.18+1371C>T
Intron_number1/9
R07D5.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1c.1:c.-165-6032C>T
Intron_number1/11
R07D5.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1a.1:c.-8-5625C>T
Intron_number1/12
R07D5.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1g.1:c.18+1371C>T
Intron_number2/11
R07D5.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1d.1:c.268-6032C>T
Intron_number1/9
R07D5.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1e.1:c.268-6032C>T
Intron_number1/10
MethodWGS_Flibotte