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WormBase Tree Display for Variation: WBVar01447216

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Name Class

WBVar01447216EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01447216
Other_nameK02D10.1c.2:c.*332+11T>A
K02D10.1b.1:c.241+11T>A
K02D10.1c.3:c.*332+11T>A
K02D10.1c.1:c.*221+11T>A
K02D10.1a.1:c.952+11T>A
HGVSgCHROMOSOME_III:g.8774495T>A
Sequence_detailsSMapS_parentSequenceK02D10
Flanking_sequencesGCTCATGTACGAGTTCATGAGTAAGTTTTTAAAAAATTGAGAATTTAAATTATAGAAAAT
Mapping_targetK02D10
Type_of_mutationSubstitutionta
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (45)
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193333760
dbSNP_ssss295509679
StatusLive
AffectsGeneWBGene00019301
WBGene00305497
TranscriptK02D10.9
K02D10.1c.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK02D10.1c.3:c.*332+11T>A
Intron_number4/4
K02D10.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK02D10.1b.1:c.241+11T>A
Intron_number3/5
K02D10.1c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK02D10.1c.2:c.*332+11T>A
Intron_number4/5
K02D10.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK02D10.1c.1:c.*221+11T>A
Intron_number5/6
K02D10.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK02D10.1a.1:c.952+11T>A
Intron_number2/4
ReferenceWBPaper00040707
MethodWGS_Andersen