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: WBVar01587120

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01587120NamePublic_nameWBVar01587120
Other_namecewivar00229456
W08A12.1a.1:c.48-1372A>C
W08A12.1c.1:c.123+2541A>C
W08A12.1b.2:c.141+2541A>C
W08A12.1e.1:c.66+2541A>C
W08A12.1b.1:c.141+2541A>C
W08A12.1b.3:c.141+2541A>C
HGVSgCHROMOSOME_V:g.3694599A>C
Sequence_detailsSMapS_parentSequenceW08A12
Flanking_sequencesGGCCTTAATAAGTTTCGAAAAAGCTTGTGTGATTTACGGGCTTTAGTCAGTTTCGAATAA
Mapping_targetW08A12
Source_location225CHROMOSOME_V36945863694586From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAC
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+2541A>C
Intron_number3/7
W08A12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1a.1:c.48-1372A>C
Intron_number2/7
W08A12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1c.1:c.123+2541A>C
Intron_number3/7
W08A12.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.2:c.141+2541A>C
Intron_number4/8
W08A12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.1:c.141+2541A>C
Intron_number4/8
W08A12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1e.1:c.66+2541A>C
Intron_number1/4
MethodWGS_Flibotte