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WormBase Tree Display for Variation: WBVar00305069

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Name Class

WBVar00305069EvidencePaper_evidenceWBPaper00036201
NamePublic_nameotn8248
Other_nameOH7677_28352
K01A2.8c.2:c.176+164A>T
K01A2.4a.2:c.*95+454T>A
K01A2.8c.3:c.176+164A>T
K01A2.8d.1:c.323+164A>T
K01A2.8c.1:c.176+164A>T
K01A2.8a.1:c.308+164A>T
HGVSgCHROMOSOME_II:g.309998T>A
Sequence_detailsSMapS_parentSequenceK01A2
Flanking_sequencesTAACACTGCCCCCCCGGCGTTACTCCACTTTTAAAATTTAAAAACCAAAATTCAGCCAAAACAATTGTCTTAATTTTAAAAAGTCTGTACCGACAATATC
Mapping_targetK01A2
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00029537
LaboratoryOTN
AnalysisWGS_Hobert
StatusLive
AffectsGeneWBGene00019279
WBGene00019282
TranscriptK01A2.8d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8d.1:c.323+164A>T
Intron_number3/4
K01A2.8c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.1:c.176+164A>T
Intron_number3/5
K01A2.8a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8a.1:c.308+164A>T
Intron_number4/6
K01A2.8c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.2:c.176+164A>T
Intron_number4/6
K01A2.8c.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.8c.3:c.176+164A>T
Intron_number4/6
K01A2.4a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK01A2.4a.2:c.*95+454T>A
Intron_number12/12
GeneticsMapII
ReferenceWBPaper00036201
MethodWGS_Hobert