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: WBVar01607467

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01607467NamePublic_nameWBVar01607467
Other_namecewivar00286543
F18F11.3g.1:c.2298+92T>C
F18F11.3d.1:c.2298+92T>C
F18F11.3e.1:c.2298+92T>C
F18F11.3b.1:c.2298+92T>C
F18F11.3h.1:c.2298+92T>C
F18F11.3c.1:c.2298+92T>C
F18F11.3f.1:c.2298+92T>C
F18F11.3a.1:c.2298+92T>C
HGVSgCHROMOSOME_IV:g.353241T>C
Sequence_detailsSMapS_parentSequenceY66H1B
Flanking_sequencesTGTAGGAGTACGGTAGGATTACCGGGGCTATGTAGGAGTACGGTAGGATTACTGTAGTTTTGAAAAAAAA
Mapping_targetY66H1B
Source_location225CHROMOSOME_IV353241353241From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (12)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00017576
TranscriptF18F11.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3e.1:c.2298+92T>C
Intron_number14/25
F18F11.3g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3g.1:c.2298+92T>C
Intron_number14/25
F18F11.3f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3f.1:c.2298+92T>C
Intron_number14/24
F18F11.3h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3h.1:c.2298+92T>C
Intron_number14/26
F18F11.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3d.1:c.2298+92T>C
Intron_number14/25
F18F11.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3a.1:c.2298+92T>C
Intron_number14/25
F18F11.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3b.1:c.2298+92T>C
Intron_number14/23
F18F11.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18F11.3c.1:c.2298+92T>C
Intron_number14/24
MethodWGS_Flibotte