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WormBase Tree Display for Variation: WBVar01448216

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Name Class

WBVar01448216EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01448216
Other_nameY39A1A.13a.1:c.920-52C>T
Y39A1A.13b.3:c.548-52C>T
Y39A1A.13b.2:c.548-52C>T
Y39A1A.13b.1:c.548-52C>T
HGVSgCHROMOSOME_III:g.10648465C>T
Sequence_detailsSMapS_parentSequenceY39A1A
Flanking_sequencesCTAATTTTCGATTATATTGATGAGAAAAAAATGAAAATTTTAAGCTTATTTTTTAAAAAT
Mapping_targetY39A1A
Type_of_mutationSubstitutionct
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (28)
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193334443
dbSNP_ssss295510362
StatusLive
AffectsGeneWBGene00012651
TranscriptY39A1A.13b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39A1A.13b.3:c.548-52C>T
Intron_number4/6
Y39A1A.13b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39A1A.13b.1:c.548-52C>T
Intron_number6/7
Y39A1A.13a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39A1A.13a.1:c.920-52C>T
Intron_number6/8
Y39A1A.13b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39A1A.13b.2:c.548-52C>T
Intron_number5/7
ReferenceWBPaper00040707
MethodWGS_Andersen