Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01756935

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01756935NamePublic_nameWBVar01756935
Other_namecewivar00456547
F25C8.3b.1:c.1096+281C>T
F25C8.3d.1:c.1096+281C>T
F25C8.3e.1:c.1096+281C>T
F25C8.3c.1:c.1042+281C>T
F25C8.3a.1:c.1096+281C>T
HGVSgCHROMOSOME_V:g.20883714C>T
Sequence_detailsSMapS_parentSequenceF25C8
Flanking_sequencesTTTGTTATTTGTACTGCATTTCCTCAAAAGTCATGTTTTTCAAAATTTTGGCAATTAAAA
Mapping_targetF25C8
Source_location225CHROMOSOME_V2088368320883683From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006812
TranscriptF25C8.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3d.1:c.1096+281C>T
Intron_number6/36
F25C8.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3b.1:c.1096+281C>T
Intron_number7/35
F25C8.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3e.1:c.1096+281C>T
Intron_number6/33
F25C8.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3c.1:c.1042+281C>T
Intron_number6/34
F25C8.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3a.1:c.1096+281C>T
Intron_number6/36
MethodWGS_Flibotte