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: WBVar01446052

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01446052EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01446052
Other_nameY42G9A.6d.1:c.343-1447C>A
Y42G9A.6e.1:c.343-1447C>A
Y42G9A.6c.1:c.382-1447C>A
Y42G9A.6a.1:c.382-1447C>A
Y42G9A.6g.1:c.292-1447C>A
Y42G9A.6f.1:c.292-1447C>A
HGVSgCHROMOSOME_III:g.6145798G>T
Sequence_detailsSMapS_parentSequenceY42G9A
Flanking_sequencesATAATTTTTTAAAGTTCTTTGAGTGAGTCCATTGGAAATAATTAAAAGTACTAGTAGTAC
Mapping_targetY42G9A
Type_of_mutationSubstitutiongt
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193332955
dbSNP_ssss295508874
StatusLive
AffectsGeneWBGene00021535
TranscriptY42G9A.6g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY42G9A.6g.1:c.292-1447C>A
Intron_number3/9
Y42G9A.6f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY42G9A.6f.1:c.292-1447C>A
Intron_number3/10
Y42G9A.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY42G9A.6c.1:c.382-1447C>A
Intron_number5/12
Y42G9A.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY42G9A.6a.1:c.382-1447C>A
Intron_number5/12
Y42G9A.6d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY42G9A.6d.1:c.343-1447C>A
Intron_number4/10
Y42G9A.6e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY42G9A.6e.1:c.343-1447C>A
Intron_number4/10
ReferenceWBPaper00040707
MethodWGS_Andersen