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: WBVar01267979

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01267979EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01267979
Other_namecewivar00023798
T21C12.1f.1:c.563-1183A>C
T21C12.1c.1:c.1165-29A>C
T21C12.1c.2:c.1165-29A>C
T21C12.1o.1:c.59-1183A>C
T21C12.1e.1:c.1222-29A>C
T21C12.1k.1:c.1165-29A>C
T21C12.1d.1:c.1129-29A>C
T21C12.1m.1:c.661-29A>C
HGVSgCHROMOSOME_III:g.10529403A>C
Sequence_detailsSMapS_parentSequenceT21C12
Flanking_sequencesGCCGGACACAATTCCTCTATGGTTAGTTTTAGAAAATAATTTTTTGGGATAAAATAATAATTTGCTGAAAATTTTCAGAATCCATTGATGGAGATCCCAG
Mapping_targetT21C12
Type_of_mutationSubstitutionaCPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (12)
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539103125
StatusLive
AffectsGeneWBGene00006784
TranscriptT21C12.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1k.1:c.1165-29A>C
Intron_number9/11
T21C12.1m.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1m.1:c.661-29A>C
Intron_number5/8
T21C12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.1:c.1165-29A>C
Intron_number10/18
T21C12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1e.1:c.1222-29A>C
Intron_number11/19
T21C12.1c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1c.2:c.1165-29A>C
Intron_number10/14
T21C12.1o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1o.1:c.59-1183A>C
Intron_number1/5
T21C12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1d.1:c.1129-29A>C
Intron_number9/17
T21C12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1f.1:c.563-1183A>C
Intron_number6/11
ReferenceWBPaper00037807
MethodWGS_De_Bono