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: WBVar01513898

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01513898NamePublic_nameWBVar01513898
Other_namecewivar00036132
Y54G2A.17a.1:c.1368+169A>G
Y54G2A.17b.1:c.1428+169A>G
Y54G2A.17a.3:c.1368+169A>G
Y54G2A.17a.2:c.1368+169A>G
HGVSgCHROMOSOME_IV:g.2875026T>C
Sequence_detailsSMapS_parentSequenceY54G2A
Flanking_sequencesTTTTCATAATTTTTTTTTTTCGTCTGAATTCTAGAAACTTGTAGTGAAAAATTGGGCTAT
Mapping_targetY54G2A
Source_location225CHROMOSOME_IV28750242875024From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (12)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021882
TranscriptY54G2A.17a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY54G2A.17a.3:c.1368+169A>G
Intron_number5/7
Y54G2A.17b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY54G2A.17b.1:c.1428+169A>G
Intron_number6/7
Y54G2A.17a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY54G2A.17a.2:c.1368+169A>G
Intron_number6/8
Y54G2A.17a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY54G2A.17a.1:c.1368+169A>G
Intron_number6/8
MethodWGS_Flibotte