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WormBase Tree Display for Variation: WBVar01259423

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Name Class

WBVar01259423EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01259423
Other_namecewivar00124283
H14E04.2b.1:c.1177+173A>G
H14E04.2d.1:c.802+173A>G
H14E04.2a.1:c.1168+173A>G
H14E04.2c.1:c.1189+173A>G
HGVSgCHROMOSOME_III:g.2382085A>G
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesCGGTGGGACCCAAAAACGGGAACATAGGCAATATGGGTGTCATTTGAAAGTCTCGATACGCTGGATTTGAATTTTTAAATAAAAATGAGCAATCACCTAA
Mapping_targetH14E04
Type_of_mutationSubstitutionaGPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (28)
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539095425
HistoryAcquires_mergeWBVar01327570
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.1168+173A>G
Intron_number8/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.1189+173A>G
Intron_number9/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.1177+173A>G
Intron_number8/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.802+173A>G
Intron_number5/8
ReferenceWBPaper00037807
MethodWGS_De_Bono