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WormBase Tree Display for Variation: WBVar00299870

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Name Class

WBVar00299870EvidencePaper_evidenceWBPaper00036201
NamePublic_nameotn3049
Other_nameOH4247_143598
T21C12.1o.1:c.602-103T>A
T21C12.1c.1:c.*543-103T>A
T21C12.1f.1:c.1106-103T>A
T21C12.1h.1:c.554-103T>A
T21C12.1e.1:c.*543-103T>A
T21C12.1i.1:c.233-103T>A
T21C12.1d.1:c.*543-103T>A
HGVSgCHROMOSOME_III:g.10532106T>A
Sequence_detailsSMapS_parentSequenceT21C12
Flanking_sequencesACTGTAGGGGTAATATAGAAGTACTGTAGTTTTAACAGAAACTAGCTTTTTAGCCGCCCATTTTTTGGCTAAAACCCATTTTTTGAGTTTCTCATGAGAA
Mapping_targetT21C12
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00029440
LaboratoryOTN
AnalysisWGS_Hobert
StatusLive
AffectsGeneWBGene00006784
TranscriptT21C12.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1h.1:c.554-103T>A
Intron_number4/6
T21C12.1o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1o.1:c.602-103T>A
Intron_number4/5
T21C12.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1i.1:c.233-103T>A
Intron_number1/2
T21C12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1d.1:c.*543-103T>A
Intron_number16/17
T21C12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.1:c.*543-103T>A
Intron_number17/18
T21C12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1e.1:c.*543-103T>A
Intron_number18/19
T21C12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1f.1:c.1106-103T>A
Intron_number9/11
GeneticsMapIII
ReferenceWBPaper00036201
MethodWGS_Hobert