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WormBase Tree Display for Variation: WBVar00307865

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Name Class

WBVar00307865EvidencePaper_evidenceWBPaper00036201
NamePublic_nameotn11044
Other_nameOH8421_70358
T08A11.1d.1:c.174+48T>C
T08A11.1c.1:c.174+48T>C
T08A11.1f.1:c.174+48T>C
T08A11.1b.1:c.174+48T>C
T08A11.1a.1:c.174+48T>C
T08A11.1g.1:c.174+48T>C
T08A11.1e.1:c.174+48T>C
T08A11.1h.1:c.174+48T>C
HGVSgCHROMOSOME_III:g.4262827A>G
Sequence_detailsSMapS_parentSequenceT08A11
Flanking_sequencesAAACCGGTCTATTGAGGTAATTTGAGTATTTTAACTTTACTTTAATTTTATTTTTCAGTATTTTAATGAATAATTCTGTGCCCTATCCATTACGAACCGG
Mapping_targetT08A11
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00029552
LaboratoryOTN
AnalysisWGS_Hobert
StatusLive
AffectsGeneWBGene00011604
TranscriptT08A11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1e.1:c.174+48T>C
Intron_number1/17
T08A11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1g.1:c.174+48T>C
Intron_number2/18
T08A11.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1h.1:c.174+48T>C
Intron_number2/18
T08A11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1d.1:c.174+48T>C
Intron_number2/18
T08A11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1f.1:c.174+48T>C
Intron_number1/17
T08A11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1c.1:c.174+48T>C
Intron_number1/17
T08A11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1b.1:c.174+48T>C
Intron_number2/18
T08A11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1a.1:c.174+48T>C
Intron_number2/18
GeneticsMapIII
ReferenceWBPaper00036201
MethodWGS_Hobert