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WormBase Tree Display for Variation: WBVar01567388

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Name Class

WBVar01567388NamePublic_nameWBVar01567388
Other_name (11)
HGVSgCHROMOSOME_III:g.10526867C>T
Sequence_detailsSMapS_parentSequenceT21C12
Flanking_sequencesGGCTGCTTCTTGAAATGCAAAGCAGATAAGGCACCTAAGAGCACCGTAGTTCAAGATTAC
Mapping_targetT21C12
Source_location225CHROMOSOME_III1052676910526769From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006784
TranscriptT21C12.1l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1l.1:c.440-54C>T
Intron_number4/8
T21C12.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1k.1:c.563-1103C>T
Intron_number5/11
T21C12.1m.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1m.1:c.59-1103C>T
Intron_number1/8
T21C12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.1:c.563-1103C>T
Intron_number6/18
T21C12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1e.1:c.563-1103C>T
Intron_number6/19
T21C12.1c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.2:c.563-1103C>T
Intron_number6/14
T21C12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1b.1:c.944-54C>T
Intron_number9/14
T21C12.1o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1o.1:c.58+2542C>T
Intron_number1/5
T21C12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1d.1:c.563-1103C>T
Intron_number6/17
T21C12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1f.1:c.562+2542C>T
Intron_number6/11
MethodWGS_Flibotte