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WormBase Tree Display for Variation: WBVar00584094

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Name Class

WBVar00584094EvidencePaper_evidenceWBPaper00038208
NamePublic_nameWBVar00584094
Other_namehaw164229
cewivar00229468
W08A12.1e.1:c.651+228G>C
W08A12.1b.2:c.726+228G>C
W08A12.1a.1:c.897+228G>C
W08A12.1b.3:c.726+228G>C
W08A12.1b.1:c.726+228G>C
W08A12.1c.1:c.708+228G>C
W08A12.1d.1:c.849+228G>C
HGVSgCHROMOSOME_V:g.3699184G>C
Sequence_detailsSMapS_parentSequenceW08A12
Flanking_sequencesGCGACTTGCCGGTTTGCCAATTTGCCGGAAATTTTCAGTTCCGCCAGTTTCCGGTTTGCCGAAAATTCTTAATTCCGGCAATTTGCCGGTGTGCCGAAAT
Mapping_targetW08A12
Type_of_mutationSubstitutiongc
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WGS_Yanai
PersonWBPerson4037
AnalysisWGS_Yanai
Million_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021078
TranscriptW08A12.1b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.3:c.726+228G>C
Intron_number5/7
W08A12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1a.1:c.897+228G>C
Intron_number5/7
W08A12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1c.1:c.708+228G>C
Intron_number5/7
W08A12.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.2:c.726+228G>C
Intron_number6/8
W08A12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.1:c.726+228G>C
Intron_number6/8
W08A12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1d.1:c.849+228G>C
Intron_number3/5
W08A12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1e.1:c.651+228G>C
Intron_number3/4
ReferenceWBPaper00038208
MethodWGS_Yanai