Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01470482

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01470482EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01470482
Other_namecewivar00060515
C23F12.1w.1:c.1215+1069G>A
C23F12.1e.1:c.1215+1069G>A
C23F12.1a.1:c.1215+1069G>A
C23F12.1t.1:c.1215+1069G>A
C23F12.1u.1:c.1215+1069G>A
C23F12.1r.1:c.1215+1069G>A
C23F12.1s.1:c.1215+1069G>A
C23F12.1v.1:c.1215+1069G>A
HGVSgCHROMOSOME_X:g.9401741G>A
Sequence_detailsSMapS_parentSequenceC23F12
Flanking_sequencesTTCATAATTGGTGTTTAAATTTGCCAATTTCGATTGAAATTTAAAATTTGAATTCAGAAA
Mapping_targetC23F12
Type_of_mutationSubstitutionga
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (77)
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193355784
dbSNP_ssss295531703
StatusLive
AffectsGeneWBGene00016006
TranscriptC23F12.1t.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC23F12.1t.1:c.1215+1069G>A
Intron_number8/49
C23F12.1v.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC23F12.1v.1:c.1215+1069G>A
Intron_number8/48
C23F12.1u.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC23F12.1u.1:c.1215+1069G>A
Intron_number8/45
C23F12.1s.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC23F12.1s.1:c.1215+1069G>A
Intron_number8/49
C23F12.1w.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC23F12.1w.1:c.1215+1069G>A
Intron_number8/44
C23F12.1r.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC23F12.1r.1:c.1215+1069G>A
Intron_number8/46
C23F12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC23F12.1a.1:c.1215+1069G>A
Intron_number9/52
C23F12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC23F12.1e.1:c.1215+1069G>A
Intron_number8/46
ReferenceWBPaper00040707
MethodWGS_Andersen