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: WBVar01853909

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01853909NamePublic_nameWBVar01853909
Other_namecewivar00567054
T09A12.4f.1:c.324-1357T>C
T09A12.4g.1:c.102-1357T>C
T09A12.4d.1:c.102-1357T>C
T09A12.4c.1:c.324-1357T>C
HGVSgCHROMOSOME_IV:g.8233193A>G
Sequence_detailsSMapS_parentSequenceT09A12
Flanking_sequencesCGTAATCGTAGCAGTGATCCTATAAGTACGAAATTGGTAGGTAGGGAATTTTCTCCGCCG
Mapping_targetT09A12
Source_location225CHROMOSOME_IV82331798233179From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00219729
WBGene00003656
TranscriptT09A12.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4c.1:c.324-1357T>C
Intron_number4/13
T09A12.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4f.1:c.324-1357T>C
Intron_number4/13
T09A12.7
T09A12.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4d.1:c.102-1357T>C
Intron_number2/10
T09A12.4g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT09A12.4g.1:c.102-1357T>C
Intron_number2/10
MethodWGS_Flibotte