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: WBVar01587118

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01587118NamePublic_nameWBVar01587118
Other_namecewivar00229452
W08A12.1b.1:c.141+1244C>T
W08A12.1b.3:c.141+1244C>T
W08A12.1b.2:c.141+1244C>T
W08A12.1e.1:c.66+1244C>T
W08A12.1c.1:c.123+1244C>T
W08A12.1a.1:c.47+1244C>T
HGVSgCHROMOSOME_V:g.3693302C>T
Sequence_detailsSMapS_parentSequenceW08A12
Flanking_sequencesGTAGCATGCAAATTCGGCAAATCTACTTTTTTGAAATTTGCGTGCTCGGCAAATTCGGCAAACTTGCCGC
Mapping_targetW08A12
Source_location225CHROMOSOME_V36932893693289From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021078
TranscriptW08A12.1b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.3:c.141+1244C>T
Intron_number3/7
W08A12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1a.1:c.47+1244C>T
Intron_number2/7
W08A12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1c.1:c.123+1244C>T
Intron_number3/7
W08A12.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.2:c.141+1244C>T
Intron_number4/8
W08A12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.1:c.141+1244C>T
Intron_number4/8
W08A12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1e.1:c.66+1244C>T
Intron_number1/4
MethodWGS_Flibotte